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		<id>http://pastdb.crg.eu/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Mirimia</id>
		<title>PastDB - User contributions [en]</title>
		<link rel="self" type="application/atom+xml" href="http://pastdb.crg.eu/w/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Mirimia"/>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/wiki/Special:Contributions/Mirimia"/>
		<updated>2026-05-12T12:31:04Z</updated>
		<subtitle>User contributions</subtitle>
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	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=446</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=446"/>
				<updated>2022-10-10T17:56:06Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: /* Protein impact */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_METRICS-araTha10.tab.gz EVENT METRICS]  - Summary statistics for the usage of each AS event. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Predicted effect of the AS event on the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3-legacy.tab.gz PROTEIN IMPACT (Legacy)] - Predicted effect of the AS event on the open reading frame of the transcript. Version v3, to use with the option --legacy in vast-tools compare. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to Protein IDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Overlap of AS events with Pfam domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Overlap of AS events with PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_CONFIG-araTha10.tab.gz SAMPLE CONFIG PLOT] - Config file with sample information used for the plot in the main panel.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=444</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=444"/>
				<updated>2021-01-21T08:26:04Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_METRICS-araTha10.tab.gz EVENT METRICS]  - Summary statistics for the usage of each AS event. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Predicted effect of the AS event on the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to Protein IDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Overlap of AS events with Pfam domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Overlap of AS events with PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_CONFIG-araTha10.tab.gz SAMPLE CONFIG PLOT] - Config file with sample information used for the plot in the main panel.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=443</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=443"/>
				<updated>2021-01-17T11:21:36Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
==== How do I cite PastDB? ====&lt;br /&gt;
If you use data from PastDB, please cite our paper in [https://genomebiology.biomedcentral.com/articles/10.1186/s13059-020-02258-y Genome Biology]:&lt;br /&gt;
&lt;br /&gt;
Martín, G., Márquez, Y., Duque, P., Irimia, M. (2021). Alternative splicing landscapes in &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt; across tissues and stress conditions highlight major functional differences with animals. Genome Biol, 22:35.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.5.1''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the gene expression (GE) of a given gene quantified? ====&lt;br /&gt;
GE quantification is also performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' maps the first 50 nucleotides of the forward read (if longer and paired end) to a library with one reference transcript per gene. GE levels are provided using the cRPKM metric (corrected [for mappability] Reads Per Kilobasepair and Million mapped reads), as detailed in [https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.1144 Labbé et al., ''Stem Cells'' 2012]. cRPKM can be converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM). Moreover, ''vast-tools'' can provide tables with TPMs and raw counts.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the main page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=About&amp;diff=442</id>
		<title>About</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=About&amp;diff=442"/>
				<updated>2021-01-17T11:21:20Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;PastDB is a database of Alternative Splicing (AS) profiles across multiple tissues and environmental conditions of &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;. PastDB contains AS events (including exon skipping, alternative 5' and 3' splice sites and retained introns). AS event identification and sequence inclusion level quantification in RNA-seq samples have been performed with [https://github.com/vastgroup/vast-tools &amp;lt;i&amp;gt;vast-tools&amp;lt;/i&amp;gt;].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
In addition to AS inclusion levels, PastDB provides general information about the AS events, including genomic and sequence context, impact on the reading frame, overlap with protein domains and disordered regions and primers for AS event validation through RT-PCR. Moreover, it also provides measures of Gene Expression, using the cRPKM metric.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
If you see an AS event that you find inconsistent, or you have any questions, comments or suggestions about the database, please do not hesitate to e-mail us to [mailto:vastdb@googlegroups.com vastdb@googlegroups.com].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
How to cite: if you use data from PastDB, please cite our paper in [https://genomebiology.biomedcentral.com/articles/10.1186/s13059-020-02258-y Genome Biology]:&lt;br /&gt;
&lt;br /&gt;
Martín, G., Márquez, Y., Duque, P., Irimia, M. (2021). Alternative splicing landscapes in &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt; across tissues and stress conditions highlight major functional differences with animals. Genome Biol, 22:35.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=441</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=441"/>
				<updated>2021-01-17T11:18:30Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
==== How do I cite PastDB? ====&lt;br /&gt;
If you use data from PastDB, please cite our paper in [https://genomebiology.biomedcentral.com/articles/10.1186/s13059-020-02258-y Genome Biology]:&lt;br /&gt;
&lt;br /&gt;
Martin, G., Márquez, Y., Duque, P., Irimia, M. (2021). Alternative splicing landscapes in &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt; across tissues and stress conditions highlight major functional differences with animals. Genome Biol, 22:35.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.5.1''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the gene expression (GE) of a given gene quantified? ====&lt;br /&gt;
GE quantification is also performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' maps the first 50 nucleotides of the forward read (if longer and paired end) to a library with one reference transcript per gene. GE levels are provided using the cRPKM metric (corrected [for mappability] Reads Per Kilobasepair and Million mapped reads), as detailed in [https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.1144 Labbé et al., ''Stem Cells'' 2012]. cRPKM can be converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM). Moreover, ''vast-tools'' can provide tables with TPMs and raw counts.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the main page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=About&amp;diff=440</id>
		<title>About</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=About&amp;diff=440"/>
				<updated>2021-01-17T11:17:01Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;PastDB is a database of Alternative Splicing (AS) profiles across multiple tissues and environmental conditions of &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;. PastDB contains AS events (including exon skipping, alternative 5' and 3' splice sites and retained introns). AS event identification and sequence inclusion level quantification in RNA-seq samples have been performed with [https://github.com/vastgroup/vast-tools &amp;lt;i&amp;gt;vast-tools&amp;lt;/i&amp;gt;].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
In addition to AS inclusion levels, PastDB provides general information about the AS events, including genomic and sequence context, impact on the reading frame, overlap with protein domains and disordered regions and primers for AS event validation through RT-PCR. Moreover, it also provides measures of Gene Expression, using the cRPKM metric.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
If you see an AS event that you find inconsistent, or you have any questions, comments or suggestions about the database, please do not hesitate to e-mail us to [mailto:vastdb@googlegroups.com vastdb@googlegroups.com].&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
How to cite: if you use data from PastDB, please cite our paper in [https://genomebiology.biomedcentral.com/articles/10.1186/s13059-020-02258-y Genome Biology]:&lt;br /&gt;
&lt;br /&gt;
Martin, G., Márquez, Y., Duque, P., Irimia, M. (2021). Alternative splicing landscapes in &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt; across tissues and stress conditions highlight major functional differences with animals. Genome Biol, 22:35.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=439</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=439"/>
				<updated>2020-11-30T15:51:34Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_METRICS-araTha10.tab.gz EVENT METRICS]  - Summary statistics for the usage of each AS event. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Predicted effect of the AS event on the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to Protein IDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Overlap of AS events with Pfam domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Overlap of AS events with PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=438</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=438"/>
				<updated>2020-11-30T15:48:54Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_METRICS-araTha10.tab.gz EVENT METRICS]  - Summary statistics for the usage of each AS event. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Effect of the AS event in the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=437</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=437"/>
				<updated>2020-11-30T15:48:37Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/hg38/EVENT_METRICS-araTha10.tab.gz EVENT METRICS]  - Summary statistics for the usage of each AS event. &lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Effect of the AS event in the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=436</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=436"/>
				<updated>2020-11-30T15:46:24Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENT INFORMATION]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI TABLE] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI TABLE] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI TABLE] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI TABLE] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI TABLE] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITE INFORMATION] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT] - Effect of the AS event in the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAIN OVERLAP (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAIN OVERLAP (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENE INFORMATION] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION TABLE] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION TABLE] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION TABLE] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION TABLE] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION TABLE] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz EVENT_ID-to-GENE_ID] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE INFORMATION] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=435</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=435"/>
				<updated>2020-11-30T15:42:26Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI table] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI table] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI table] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI table] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PRIMER SUGGESTIONS table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION table] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION table] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION table] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION table] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=434</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=434"/>
				<updated>2020-11-30T15:26:05Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.5.1''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the gene expression (GE) of a given gene quantified? ====&lt;br /&gt;
GE quantification is also performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' maps the first 50 nucleotides of the forward read (if longer and paired end) to a library with one reference transcript per gene. GE levels are provided using the cRPKM metric (corrected [for mappability] Reads Per Kilobasepair and Million mapped reads), as detailed in [https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.1144 Labbé et al., ''Stem Cells'' 2012]. cRPKM can be converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM). Moreover, ''vast-tools'' can provide tables with TPMs and raw counts.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the main page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=433</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=433"/>
				<updated>2020-11-05T11:42:44Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples, using the cRPKM metric. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; cRPKM can be converted to TPMs applying the following formula: TPM &amp;amp;#61 10^6 * cRPKM/sum_all(cRPKM).&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=432</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=432"/>
				<updated>2020-11-05T11:42:04Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples, using the cRPKM metric. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; cRPKM can be converted to TPMs applying the following formula: TPM &amp;amp;equals 10^6 * cRPKM/sum_all(cRPKM).&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=431</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=431"/>
				<updated>2020-11-05T10:13:50Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI table] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI table] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI table] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI table] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION table] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION table] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION table] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION table] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=430</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=430"/>
				<updated>2020-11-05T09:56:38Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples, using the cRPKM metric. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; cRPKM can be converted to TPMs applying the following formula: TPM '=' 10^6 * cRPKM/sum_all(cRPKM).&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=429</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=429"/>
				<updated>2020-11-05T09:55:42Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples, using the cRPKM metric. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; cRPKM can be converted to TPMs applying the following formula: TPM \= 10\^6 \* cRPKM\/sum_all(cRPKM).&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=428</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=428"/>
				<updated>2020-11-05T09:54:47Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.5.1''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the gene expression (GE) of a given gene quantified? ====&lt;br /&gt;
GE quantification is also performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' maps the first 50 nucleotides of the forward read (if longer and paired end) to a library with one reference transcript per gene. GE levels are provided using the cRPKM metric (corrected [for mappability] Reads Per Kilobasepair and Million mapped reads), as detailed in [https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.1144 Labbé et al., ''Stem Cells'' 2012]. cRPKM can be converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM). Moreover, ''vast-tools'' can provide tables with TPMs and raw counts.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=427</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=427"/>
				<updated>2020-11-05T09:54:33Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples, using the cRPKM metric. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; cRPKM can be converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM).&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=426</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=426"/>
				<updated>2020-11-05T09:52:09Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.5.1''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the gene expression (GE) of a given gene quantified? ====&lt;br /&gt;
GE quantification is also performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' maps the first 50 nucleotides of the forward read (if longer and paired end) to a library with one reference transcript per gene. GE levels are provided using the cRPKM metric (corrected [for mappability] Reads Per Kilobasepair and Million mapped reads), as detailed in [https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1002/stem.1144 Labbé et al., ''Stem Cells'' 2012]. cRPKM can be easily converted to TPMs applying the following formula: TPM = 10^6 * cRPKM/sum_all(cRPKM). Moreover, ''vast-tools'' can provide tables with TPMs and raw counts.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=425</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=425"/>
				<updated>2020-11-05T09:43:20Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI table] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI table] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI table] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI table] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v2.3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v2.3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz MAIN EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION table] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION table] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION table] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION table] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=424</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=424"/>
				<updated>2020-11-05T09:42:47Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz MAIN PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC-v251.tab.gz ABIOTIC PSI table] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC-v251.tab.gz BIOTIC PSI table] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT-v251.tab.gz LIGHT PSI table] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS-v251.tab.gz SPL_FACTORS PSI table] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v2.3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v2.3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz ABIOTIC EXPRESSION table] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz BIOTIC EXPRESSION table] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz LIGHT EXPRESSION table] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz SPL_FACTORS EXPRESSION table] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=423</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=423"/>
				<updated>2020-11-05T09:39:32Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{#vardefine:server|http://vastdb.crg.eu}}From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages (main PSI plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-40-ABIOTIC.tab.gz PSI table] - Inclusion patterns of AS events in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-18-BIOTIC.tab.gz PSI table] - Inclusion patterns of AS events in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-21-LIGHT.tab.gz PSI table] - Inclusion patterns of AS events in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PSI_TABLE-araTha10-33-SPL_FACTORS.tab.gz PSI table] - Inclusion patterns of AS events upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_IMPACT-araTha10-v2.3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v2.3.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads (main GE plot).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-40-ABIOTIC-NORM.tab.gz PSI table] - Gene expression in ABIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-18-BIOTIC-NORM.tab.gz PSI table] - Gene expression in BIOTIC stress experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-21-LIGHT-NORM.tab.gz PSI table] - Gene expression in LIGHT experiments (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/cRPKM-araTha10-33-SPL_FACTORS-NORM.tab.gz PSI table] - Gene expression upon SPLICING FACTOR disruption (special dataset).&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{#var:server}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=399</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=399"/>
				<updated>2020-07-02T16:13:43Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.2.2''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=398</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=398"/>
				<updated>2020-07-02T16:12:53Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.2.2''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
&amp;quot;Domain information is currently available for cassette exons as well as for adjacent constitutive regions for INT, ALTA and ALTD events.&amp;quot;&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Publications&amp;diff=397</id>
		<title>Publications</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Publications&amp;diff=397"/>
				<updated>2020-07-02T15:57:33Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
&lt;br /&gt;
====  PastDB publication ====&lt;br /&gt;
* Martín, G., Marquez, Y., Duque, P., Irimia, M. (2020). Alternative splicing landscapes in Arabidopsis thaliana across tissues and stress conditions highlight major functional differences with animals. Submitted.&lt;br /&gt;
&lt;br /&gt;
====  VastDB publication (v1.0) ====&lt;br /&gt;
* Tapial, J., Ha, K. C. H., Sterne-Weiler, T., Gohr, A., Braunschweig, U., Hermoso-Pulido, A., Quesnel-Vallières, M., Permanyer, J., Sodaei, R., Marquez, Y., Cozzuto, L., Wang, X., Gómez-Velázquez, M., Rayon, T., Manzanares, M., Ponomarenko, J., Blencowe, B. J., Irimia, M. (2017). An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms. ''Genome Research, 27''(10), 1759–1768. [[http://genome.cshlp.org/content/27/10/1759.long link]] [[https://www.ncbi.nlm.nih.gov/pubmed/28855263 PubMed]]&lt;br /&gt;
&lt;br /&gt;
==== vast-tools  ====&lt;br /&gt;
* Tapial, J., Ha, K. C. H., Sterne-Weiler, T., Gohr, A., Braunschweig, U., Hermoso-Pulido, A., Quesnel-Vallières, M., Permanyer, J., Sodaei, R., Marquez, Y., Cozzuto, L., Wang, X., Gómez-Velázquez, M., Rayon, T., Manzanares, M., Ponomarenko, J., Blencowe, B. J., Irimia, M. (2017). An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms. ''Genome Research, 27''(10), 1759–1768. [[http://genome.cshlp.org/content/27/10/1759.long link]] [[https://www.ncbi.nlm.nih.gov/pubmed/28855263 PubMed]]&lt;br /&gt;
&lt;br /&gt;
* Irimia, M., Weatheritt, R.J., Ellis, J., Parikshak, N.N., Gonatopoulos-Pournatzis, T., Babor, M., Quesnel-Vallières, M., Tapial, J., Raj, B., O’Hanlon, D., Barrios-Rodiles, M., Sternberg, M.J.E., Cordes, S.P., Roth, F.P., Wrana, J.L., Geschwind, D.H., Blencowe, B.J. (2014). A highly conserved program of neuronal microexons is misregulated in autistic brains. ''Cell'', 59:1511-23. [[http://www.cell.com/abstract/S0092-8674(14)01512-8 link]] [[http://www.ncbi.nlm.nih.gov/pubmed/25525873 PubMed]]&lt;br /&gt;
&lt;br /&gt;
==== Intron retention analysis ====&lt;br /&gt;
* Braunschweig, U., Barbosa-Morais, N.L., Pan, Q., Nachman, E., Alipahani, B., Gonatopoulos-Pournatzis, T., Frey, B., Irimia, M., Blencowe, B.J. (2014). Widespread intron retention in mammals functionally tunes transcriptomes. ''Genome Research'', 24:1774-86. [[http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 link]] [[http://www.ncbi.nlm.nih.gov/pubmed/25258385 PubMed]]&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=377</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=377"/>
				<updated>2020-06-30T21:34:20Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Template:Event&amp;diff=351</id>
		<title>Template:Event</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Template:Event&amp;diff=351"/>
				<updated>2020-06-29T08:34:01Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
&amp;lt;includeonly&amp;gt;{{#vardefine:id|{{#cleanTag:{{FULLPAGENAMEE}}|at|pre}}}}{{#vardefine:genome|{{#cleanTag:{{FULLPAGENAMEE}}|pre}}}}{{BioDB_oldid|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;nowiki /&amp;gt;{{DISPLAYTITLE:{{#var:id|}}}}{{#CustomMsg:Help:Event.ini|ini}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
''{{TypeEvent|{{PAGENAME}}}}''&amp;lt;nowiki /&amp;gt;{{BioDB_event|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
{{BioDB_event_metrics|{{#var:id}}}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;tablebox event-assembly&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Gene&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{#ifeq:{{#var:gene_id|}}||NA|[[Gene:{{#var:gene_id|}}@Genome:{{#var:genome|}}|{{#var:gene_id|}}]]&lt;br /&gt;
}}{{#ifeq:{{#var:gene_name|}}|||&amp;amp;nbsp;{{!}} ''{{#var:gene_name|}}'' }}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Description&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{#if:{{#var:description|}}|{{#var:description|}}|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Coordinates&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span class='genome-nor'&amp;gt;{{#var:chro_c|}}:{{#var:start_c|}}-{{#var:end_c|}}:{{#var:strand_c|}}&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-coords|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord C1 exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_c1|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord A exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_a|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord C2 exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_c2|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
		&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Length&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large=8 columns&amp;quot;&amp;gt;{{#var:length_n|}} bp{{HelpLinkedPage|type=helpicon|msg=event-length|output=data-tooltip}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Sequences&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Splice sites&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-splice|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
                         {{Score_SS|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Exon sequences&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-exon|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq C1 exon&amp;lt;/div&amp;gt;{{#var:seq_c1|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq A exon&amp;lt;/div&amp;gt;{{#var:seq_a|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq C2 exon&amp;lt;/div&amp;gt;{{#var:seq_c2|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;		&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;VastDB Features&amp;lt;/div&amp;gt;{{BioDB_mappability|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Vast-tools module Information&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-vastdbfeatures|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Secondary ID&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:oldid|}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-internal|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Average complexity&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:complex|}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-complexity|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Mappability confidence:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#ifeq:{{#var:minc|}}||NA|{{#var:minc|}}%={{#var:mexc1|}}={{#var:mexc2|}}%}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-mappability|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Protein Impact&amp;lt;/div&amp;gt;{{BioDB_protimpact|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;&amp;quot;&amp;gt;{{#var:protimpact|No protein impact description available}}{{HelpLinkedPage|type=helpicon|msg=event-impact|output=data-tooltip}}&lt;br /&gt;
{{PDBshow|{{#var:id|}}}}&lt;br /&gt;
                &amp;lt;/div&amp;gt;{{BioDB_protdisorder|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Features&amp;lt;/span&amp;gt;&lt;br /&gt;
&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Disorder rate:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;C1={{#var:c1dis|NA}} A={{#var:adis|NA}} C2={{#var:c2dis|NA}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-disorder|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
                                &amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;block&amp;quot; style=&amp;quot;display:block !important&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;body&amp;quot; style=&amp;quot;display:block !important&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;amp;nbsp;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin disorder-img&amp;quot;&amp;gt;&lt;br /&gt;
{{#BioDB:prosite_url|{{#var:id|}},DISORDER}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|DISORDER}}{{#BioDB_clear:}}&lt;br /&gt;
&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Domain overlap (PROSITE):&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&lt;br /&gt;
					&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;{{BioDB_prosite|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
						&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Info&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-prosite|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C1:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c1prosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;A:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:aprosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C2:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c2prosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin prosite-img&amp;quot;&amp;gt;{{#BioDB:prosite_url|{{#var:id|}},PROSITE}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|PROSITE}}{{#BioDB_clear:}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;/div&amp;gt;&lt;br /&gt;
					&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Domain overlap (PFAM):&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&lt;br /&gt;
					&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;{{BioDB_pfam|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
						&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Info&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-pfam|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C1:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c1pfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;A:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:apfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C2:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c2pfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin pfam-img&amp;quot;&amp;gt;{{#BioDB:prosite_url|{{#var:id|}},PFAM}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|PFAM}}{{#BioDB_clear:}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;/div&amp;gt;&lt;br /&gt;
					&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;{{BioDB_ppi|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Degree:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:degree|NA}}&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Betweeness:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:betweenness|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-degree|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Associated events&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{Associated|{{#var:id|}}|{{#var:genome|}}}}{{HelpLinkedPage|type=helpicon|msg=event-associated|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4&amp;quot;&amp;gt;Conservation&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-conservation|output=data-tooltip}}{{ConservationFull|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;{{BioDB primer|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Primers PCR&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Suggestions for RT-PCR validation&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-primers|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;F: &amp;lt;/div&amp;gt;{{#ifeq:{{#var:primerf|}}||&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;No suggested primer sequences&amp;lt;/div&amp;gt;|&amp;lt;div class=&amp;quot;contentin bioseq&amp;quot;&amp;gt;{{#var:primerf|}}&amp;lt;/div&amp;gt;}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;R: &amp;lt;/div&amp;gt;{{#ifeq:{{#var:primerr|}}||&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;No suggested primer sequences&amp;lt;/div&amp;gt;|&amp;lt;div class=&amp;quot;contentin bioseq&amp;quot;&amp;gt;{{#var:primerr|}}&amp;lt;/div&amp;gt;}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Band lengths: &amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#ifeq:{{#var:pskipping|}}|||{{#var:pskipping|}}-{{#var:pinclusion|}}}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Annotated function&amp;lt;div class=&amp;quot;submitfunction&amp;quot;&amp;gt;[[EventFunction|(Submit a function)]]&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{AnnotatedFunction|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;/div&amp;gt;		&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;br /&amp;gt;&lt;br /&gt;
====GENOMIC CONTEXT====&lt;br /&gt;
&amp;lt;div class=&amp;quot;content large-12&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;float:right&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-browser|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;browser-container genome-nor&amp;quot;&amp;gt;&lt;br /&gt;
{{#embedUCSC:chrom={{#var:chro_c|}}|start={{#var:start_c|}}|end={{#var:end_c|}}|genome_id={{#var:genome|}}}}&amp;lt;/div&amp;gt;&lt;br /&gt;
====INCLUSION PATTERN====&lt;br /&gt;
&amp;lt;div class=&amp;quot;tissuevalue-list sample-chart&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-tissuevalue|output=data-tooltip}}&amp;lt;/div&amp;gt;{{#printCharts:}}&lt;br /&gt;
&amp;lt;hr&amp;gt;&lt;br /&gt;
{{#specialImages:{{#var:id|}}|{{#var:genome|}}|AS_ABIOTIC,AS_BIOTIC,AS_LIGHT,AS_SPL_FACTORS|Abiotic stress,Biotic stress,Light response,RNA-processing factors|{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-abiotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-biotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-light|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-spl_factors|output=data-tooltip}}}}&lt;br /&gt;
&lt;br /&gt;
&amp;lt;!--{{SpecialPSIDiv}}--&amp;gt;&lt;br /&gt;
{{Event Links|{{#var:genome}}|{{#var:gene_id}}|{{#var:gene_name}}}}&lt;br /&gt;
{{PDBdiv|{{#var:genome|}}}}[[Category:Events]][[Category:Events in Genome:{{#var:genome|}}]]&amp;lt;nowiki /&amp;gt;&amp;lt;/includeonly&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=333</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=333"/>
				<updated>2020-06-22T20:06:31Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information. &amp;lt;li&amp;gt;PSI Average: average for all the samples included in the plot. &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt; Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample. Dot colors represent sample groups from a similar biological origin (see legend below). &amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/li&amp;gt;&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=332</id>
		<title>Help:Gene.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Gene.ini&amp;diff=332"/>
				<updated>2020-06-22T20:01:14Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;gene-coords=Genomic coordinates of the gene (1-based).&lt;br /&gt;
&lt;br /&gt;
gene-browser=&amp;lt;p&amp;gt;Genomic context of the gene. Click on the image to view the gene, its events and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to PastDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-expression=&amp;lt;p&amp;gt;Each of the dots in this plot represents the average expression of the gene across several related samples. Put your mouse on each dot to see the individual values for each sample.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt; Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialdataset-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various RNA-processing factors in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al. &amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-associatedevents=&amp;lt;p&amp;gt;Events belonging to the gene of interest. You can click on each of the table columns to sort the events by this column or on each of the events to access to detailed information.&lt;br /&gt;
- PSI Average: average for all the samples included in the plot.&lt;br /&gt;
- PSI Range: difference between the maximum and minimum PSIs for all the samples displayed in the plot.&lt;br /&gt;
Each of the dots in the plot represents the average PSI of the AS event across several related samples. Hover the mouse over each dot to see the individual values for each sample.&lt;br /&gt;
Dot colors represent sample groups from a similar biological origin (see legend below).&lt;br /&gt;
Samples can be included/excluded from the plot using the buttons “Show All Tissues”,”Show None Tissues”,”Select All Tissues”,”Select None Tissues”, or clicking on the sample groups below. To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-multievent=&amp;lt;p&amp;gt;Each colored line corresponds to one of the AS events in this gene (see &amp;quot;Associated Events&amp;quot;, above). Each dot corresponds to the average PSI value of the event across several related samples (as in the Gene Expression section, above). To see the individual values for an event, click on the event ID&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Events can be toggled on and off with the buttons &amp;quot;Select All Events&amp;quot; and &amp;quot;Select No Events&amp;quot;, or by clicking on the boxes next to the event names.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be toggled on and off with the buttons &amp;quot;Select All Tissues&amp;quot; and &amp;quot;Select No Tissues&amp;quot;, or by clicking on the sample groups below.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
gene-homology=&amp;lt;p&amp;gt;Homologous genes listed in Ensembl&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Event.ini&amp;diff=331</id>
		<title>Help:Event.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Event.ini&amp;diff=331"/>
				<updated>2020-06-22T19:52:50Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;event-coords=Genomic coordinates of the AS event (1-based).&lt;br /&gt;
&lt;br /&gt;
event-length=Length of the alternatively spliced sequence.&amp;lt;br&amp;gt;In ALTD/ALTA events, the most internal splice site within each event (indicated as 1/N) has a length of 0 nt, by definition.&lt;br /&gt;
&lt;br /&gt;
event-splice=Nucleotide sequences at the intron-exon boundaries. 5' splice site sequences include three exonic and six intronic positions, whereas 3' splice site sequences include 20 intronic and 3 exonic positions. Splice-site scores were calculated using MaxEntScan for the human models (more information in FAQs).&lt;br /&gt;
&lt;br /&gt;
event-exon=Nucleotide sequences of the C1, A and C2 exons. Click on the arrow to reveal the sequences.&lt;br /&gt;
&lt;br /&gt;
event-vastdbfeatures=Click on the arrow to reveal more information.&lt;br /&gt;
event-internal=Internal vast-tools ID for the event. More information in FAQs.&lt;br /&gt;
&lt;br /&gt;
event-complexity=Detailed classification of the AS event (including exon skipping, intron retention and alternative splice sites) based on its associated transcriptomic complexity. It has implication for PCR validations. See FAQs for more information.&lt;br /&gt;
&lt;br /&gt;
event-mappability=Estimate of the percent of possible closest exon-exon junctions that can be mapped uniquely using RNA-seq (ideally 100%&amp;amp;equals;100%&amp;amp;equals;100%, for exclusion junctions, upstream inclusion junctions, and downstream inclusion junctions, respectively). For a cassette exon to be included in vast-tools their reference exon-exon junctions (those formed by the neighboring exons [C1,C2] and the alternative [A] exon) must be uniquely mappable.&lt;br /&gt;
&lt;br /&gt;
event-impact=&amp;lt;p&amp;gt;Effect of the exon inclusion on the open reading frame of the transcript. &amp;lt;q&amp;gt;Ref&amp;lt;/q&amp;gt; or &amp;lt;q&amp;gt;No Ref&amp;lt;/q&amp;gt; indicates whether the exon is included in the reference mRNA of the gene. More information in the FAQ.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-disorder=Fraction of residues predicted as disordered by disopred2 in the C1, A and C2 exons.&lt;br /&gt;
&lt;br /&gt;
event-prosite=The field follows the scheme: &amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt;(&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt;), where:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt; is the domain ID in either PROSITE or PFAM databases. For PROSITE, domains with high frequency motifs (i.e. those starting with P0*) are excluded.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt; is the domain name as provided by PROSITE or PFAM databases.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt; describes the way in whcih an exon can overlap a protein domain. The possible values are:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;FE (Full Exon): The whole exonic sequence fully overlaps with a domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;WD (Whole Domain): The whole domain is fully encoded within an exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PU (Partial Upstream): The upstream (5') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PD (Partial Downstream): The downstream (3') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt; is the percentage of the domain encoded by the exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt; is the percentage of the exon that overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-pfam=The field follows the scheme: &amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt;(&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt;), where:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt; is the domain ID in either PROSITE or PFAM databases. For PROSITE, domains with high frequency motifs (i.e. those starting with P0*) are excluded.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt; is the domain name as provided by PROSITE or PFAM databases.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt; describes the way in whcih an exon can overlap a protein domain. The possible values are:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;FE (Full Exon): The whole exonic sequence fully overlaps with a domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;WD (Whole Domain): The whole domain is fully encoded within an exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PU (Partial Upstream): The upstream (5') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PD (Partial Downstream): The downstream (3') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt; is the percentage of the domain encoded by the exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt; is the percentage of the exon that overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-degree=&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;The &amp;lt;b&amp;gt;degree&amp;lt;/b&amp;gt; is defined as the number of interactions of a protein. It defines how connected, and hence important a protein is in the network. These degree values were obtained for each protein using BioGrid data.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;The &amp;lt;b&amp;gt;betweenness&amp;lt;/b&amp;gt; is defined as the number of pairwise shortest paths between all pairs of nodes in a PPI network that go through a protein, and therefore reflects the extent of centrality or &amp;lt;q&amp;gt;hubness&amp;lt;/q&amp;gt; of the protein. Hub proteins have much higher betweenness, as they connect multiple parts within a PPI network. In contrast, peripheral proteins that sit on the borders of a PPI network have lower betweenness.&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;&amp;lt;b&amp;gt;Data source:&amp;lt;/b&amp;gt; Ellis &amp;lt;i&amp;gt;et al.&amp;lt;/i&amp;gt;, Mol Cell (2012). &amp;lt;p&amp;gt;For non-human and non-mouse data, the degree and betweenness corresponds to that of the human ortholog.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-associated=AS events in the same assembly, with coordinates overlapping with this event.&lt;br /&gt;
&lt;br /&gt;
event-conservation=Orthologous events in other species, obtained by synteny conservation using LiftOver.&lt;br /&gt;
&lt;br /&gt;
event-primers=Designed in C1 and C2 exons. The band sizes correspond to the size of the two predicted bands for the specific AS event, and are optimized to reduce the impact of PCR amplification biases (more information in FAQs). Please note that if there are associated events (particularly Alt3 or Alt5) and/or the event is composed by multiple AS exons, the resulting PCR product may be much more complex and thus RT-PCR validations may not be informative. It is suggested you always take a look at the genome browser to know what it is being amplified. &lt;br /&gt;
&lt;br /&gt;
event-browser=&amp;lt;p&amp;gt;Genomic context of the event. Click on the image to view the event and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to VASTDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-tissuevalue=Each of the dots in this plot represents the average PSI of the AS event across several related samples. Put your mouse on each dot to see the individual values for each sample.&amp;lt;p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;To access to each sample information, click on the sample name of the “Show All” section.&amp;lt;p&amp;gt;Read coverage stringency is increasingly strict from 0 to 3 (PSIs for '0' are NOT reliable). This refers to the first coverage score in the vast-tools output (see the FAQ section for details). N&amp;amp;equals;0, VLOW&amp;amp;equals;1, LOW&amp;amp;equals;2, OK/SOK&amp;amp;equals;3. For information on other quality scores associated with each sample's PSI in the plot, please visit the FAQ section.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various regulators in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Help:Event.ini&amp;diff=330</id>
		<title>Help:Event.ini</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Help:Event.ini&amp;diff=330"/>
				<updated>2020-06-22T19:50:53Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;event-coords=Genomic coordinates of the AS event (1-based).&lt;br /&gt;
&lt;br /&gt;
event-length=Length of the alternatively spliced sequence.&amp;lt;br&amp;gt;In ALTD/ALTA events, the most internal splice site within each event (indicated as 1/N) has a length of 0 nt, by definition.&lt;br /&gt;
&lt;br /&gt;
event-splice=Nucleotide sequences at the intron-exon boundaries. 5' splice site sequences include three exonic and six intronic positions, whereas 3' splice site sequences include 20 intronic and 3 exonic positions. Splice-site scores were calculated using MaxEntScan for the human models (more information in FAQs).&lt;br /&gt;
&lt;br /&gt;
event-exon=Nucleotide sequences of the C1, A and C2 exons. Click on the arrow to reveal the sequences.&lt;br /&gt;
&lt;br /&gt;
event-vastdbfeatures=Click on the arrow to reveal more information.&lt;br /&gt;
event-internal=Internal vast-tools ID for the event. More information in FAQs.&lt;br /&gt;
&lt;br /&gt;
event-complexity=Detailed classification of the AS event (including exon skipping, intron retention and alternative splice sites) based on its associated transcriptomic complexity. It has implication for PCR validations. See FAQs for more information.&lt;br /&gt;
&lt;br /&gt;
event-mappability=Estimate of the percent of possible closest exon-exon junctions that can be mapped uniquely using RNA-seq (ideally 100%&amp;amp;equals;100%&amp;amp;equals;100%, for exclusion junctions, upstream inclusion junctions, and downstream inclusion junctions, respectively). For a cassette exon to be included in vast-tools their reference exon-exon junctions (those formed by the neighboring exons [C1,C2] and the alternative [A] exon) must be uniquely mappable.&lt;br /&gt;
&lt;br /&gt;
event-impact=&amp;lt;p&amp;gt;Effect of the exon inclusion on the open reading frame of the transcript. &amp;lt;q&amp;gt;Ref&amp;lt;/q&amp;gt; or &amp;lt;q&amp;gt;No Ref&amp;lt;/q&amp;gt; indicates whether the exon is included in the reference mRNA of the gene. More information in the FAQ.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-disorder=Fraction of residues predicted as disordered by disopred2 in the C1, A and C2 exons.&lt;br /&gt;
&lt;br /&gt;
event-prosite=The field follows the scheme: &amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt;(&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt;), where:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt; is the domain ID in either PROSITE or PFAM databases. For PROSITE, domains with high frequency motifs (i.e. those starting with P0*) are excluded.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt; is the domain name as provided by PROSITE or PFAM databases.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt; describes the way in whcih an exon can overlap a protein domain. The possible values are:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;FE (Full Exon): The whole exonic sequence fully overlaps with a domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;WD (Whole Domain): The whole domain is fully encoded within an exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PU (Partial Upstream): The upstream (5') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PD (Partial Downstream): The downstream (3') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt; is the percentage of the domain encoded by the exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt; is the percentage of the exon that overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-pfam=The field follows the scheme: &amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt;(&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt;&amp;amp;equals;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt;), where:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_ID&amp;lt;/i&amp;gt; is the domain ID in either PROSITE or PFAM databases. For PROSITE, domains with high frequency motifs (i.e. those starting with P0*) are excluded.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Dom_Name&amp;lt;/i&amp;gt; is the domain name as provided by PROSITE or PFAM databases.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;Type_Overlap&amp;lt;/i&amp;gt; describes the way in whcih an exon can overlap a protein domain. The possible values are:&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;FE (Full Exon): The whole exonic sequence fully overlaps with a domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;WD (Whole Domain): The whole domain is fully encoded within an exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PU (Partial Upstream): The upstream (5') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;PD (Partial Downstream): The downstream (3') of the exon overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Dom_Overlap&amp;lt;/i&amp;gt; is the percentage of the domain encoded by the exon&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;i&amp;gt;%Exon_Overlap&amp;lt;/i&amp;gt; is the percentage of the exon that overlaps the domain&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-degree=&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;The &amp;lt;b&amp;gt;degree&amp;lt;/b&amp;gt; is defined as the number of interactions of a protein. It defines how connected, and hence important a protein is in the network. These degree values were obtained for each protein using BioGrid data.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;The &amp;lt;b&amp;gt;betweenness&amp;lt;/b&amp;gt; is defined as the number of pairwise shortest paths between all pairs of nodes in a PPI network that go through a protein, and therefore reflects the extent of centrality or &amp;lt;q&amp;gt;hubness&amp;lt;/q&amp;gt; of the protein. Hub proteins have much higher betweenness, as they connect multiple parts within a PPI network. In contrast, peripheral proteins that sit on the borders of a PPI network have lower betweenness.&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;&amp;lt;b&amp;gt;Data source:&amp;lt;/b&amp;gt; Ellis &amp;lt;i&amp;gt;et al.&amp;lt;/i&amp;gt;, Mol Cell (2012). &amp;lt;p&amp;gt;For non-human and non-mouse data, the degree and betweenness corresponds to that of the human ortholog.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-associated=AS events in the same assembly, with coordinates overlapping with this event.&lt;br /&gt;
&lt;br /&gt;
event-conservation=Orthologous events in other species, obtained by synteny conservation using LiftOver.&lt;br /&gt;
&lt;br /&gt;
event-primers=Designed in C1 and C2 exons. The band sizes correspond to the size of the two predicted bands for the specific AS event, and are optimized to reduce the impact of PCR amplification biases (more information in FAQs). Please note that if there are associated events (particularly Alt3 or Alt5) and/or the event is composed by multiple AS exons, the resulting PCR product may be much more complex and thus RT-PCR validations may not be informative. It is suggested you always take a look at the genome browser to know what it is being amplified. &lt;br /&gt;
&lt;br /&gt;
event-browser=&amp;lt;p&amp;gt;Genomic context of the event. Click on the image to view the event and its context in the UCSC website&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Track colors:&amp;lt;/p&amp;gt;&amp;lt;ul&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Black:&amp;lt;/b&amp;gt; Group of neighboring cassette exon events (no link to VASTDB)&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Blue:&amp;lt;/b&amp;gt; Simple cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Purple:&amp;lt;/b&amp;gt; Cassette exon events of intermediate complexity&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Red:&amp;lt;/b&amp;gt; Complex cassette exon events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Orange:&amp;lt;/b&amp;gt; Intron retention events&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Dark green:&amp;lt;/b&amp;gt;Alternative 3' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;li&amp;gt;&amp;lt;b&amp;gt;Light green:&amp;lt;/b&amp;gt;Alternative 5' splice site choice event.&amp;lt;/li&amp;gt;&amp;lt;/ul&amp;gt;&amp;lt;p&amp;gt;See the FAQ section for further explanation.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-tissuevalue=Each of the dots in this plot represents the average PSI of the AS event across several related samples. Put your mouse on each dot to see the individual values for each sample.&amp;lt;p&amp;gt;&amp;lt;p&amp;gt;Dot colors represent sample groups from a similar biological origin (see legend below).&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Samples can be included/excluded from the plot using the buttons &amp;quot;Show All&amp;quot;,&amp;quot;Show None&amp;quot;,&amp;quot;Select All&amp;quot;,&amp;quot;Select None&amp;quot;, or clicking on the sample groups below.&amp;lt;/p&amp;gt;&amp;lt;p&amp;gt;Read coverage stringency is increasingly strict from 0 to 3 (PSIs for '0' are NOT reliable). This refers to the first coverage score in the vast-tools output (see the FAQ section for details). N&amp;amp;equals;0, VLOW&amp;amp;equals;1, LOW&amp;amp;equals;2, OK/SOK&amp;amp;equals;3. For information on other quality scores associated with each sample's PSI in the plot, please visit the FAQ section.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-abiotic=&amp;lt;p&amp;gt;Abiotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-biotic=&amp;lt;p&amp;gt;Biotic stress conditions in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-light=&amp;lt;p&amp;gt;Responses to light changes in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;br /&gt;
&lt;br /&gt;
event-specialpsi-spl_factors=&amp;lt;p&amp;gt;Experimental manipulation of various regulators in &amp;lt;i&amp;gt;A. thaliana&amp;lt;/i&amp;gt;. Sample information is available in the Supplemental Table 1 of Martín et al.&amp;lt;/p&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Template:Gene&amp;diff=329</id>
		<title>Template:Gene</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Template:Gene&amp;diff=329"/>
				<updated>2020-06-22T19:48:47Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&amp;lt;includeonly&amp;gt;{{#vardefine:id|{{#cleanTag:{{FULLPAGENAMEE}}|at|pre}}}}{{#vardefine:genome|{{#cleanTag:{{FULLPAGENAMEE}}|pre}}}}{{BioDB_gene|{{#var:id}}}}&lt;br /&gt;
__NOTOC__&lt;br /&gt;
&amp;lt;nowiki /&amp;gt;{{DISPLAYTITLE:{{#var:id}}}}{{#CustomMsg:Help:Gene.ini|ini}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;tablebox&amp;quot; id=&amp;quot;gene&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;label&amp;quot;&amp;gt;Biotype&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;content&amp;quot;&amp;gt;{{#var:type|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;label&amp;quot;&amp;gt;Gene Symbol&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;content&amp;quot;&amp;gt;''{{#var:name|}}''&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;label&amp;quot;&amp;gt;Description&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;content&amp;quot;&amp;gt;{{#var:desc|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;label&amp;quot;&amp;gt;Coordinates&amp;lt;/div&amp;gt;{{#vardefine:ref_id|Chromosome:{{#var:chro|}}@Genome:{{#var:genome}}}}&lt;br /&gt;
&amp;lt;div class=&amp;quot;content&amp;quot;&amp;gt;{{#var:chro|}}:{{#var:start|}}-{{#var:end|}}:{{#var:strand|}}{{HelpLinkedPage|type=helpicon|msg=gene-coords|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;label&amp;quot;&amp;gt;Assembly&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;content&amp;quot;&amp;gt;{{#alink:href=Genome:{{#var:genome|}}|{{#var:genome|}}}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==== GENOMIC BROWSER ====&lt;br /&gt;
&amp;lt;div style=&amp;quot;float:right&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=gene-browser|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
{{#embedUCSC:chrom={{#var:ref_id|}}|start={{#var:start|}}|end={{#var:end|}}|genome_id={{#var:genome|}}}}&lt;br /&gt;
&amp;lt;hr&amp;gt;&lt;br /&gt;
==== EXPRESSION VALUES ====&lt;br /&gt;
&amp;lt;div style=&amp;quot;float:right&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=gene-expression|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;expressionvalue-list sample-chart&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;{{#printCharts:}}&lt;br /&gt;
&amp;lt;hr&amp;gt;&lt;br /&gt;
{{#specialImages:{{#var:id|}}|{{#var:genome|}}|GE_ABIOTIC,GE_BIOTIC,GE_LIGHT,GE_SPL_FACTORS|Abiotic stress,Biotic stress,Light response,RNA-processing factors|{{HelpLinkedPage|type=helpicon|msg=gene-specialdataset-abiotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=gene-specialdataset-biotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=gene-specialdataset-light|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=gene-specialdataset-spl_factors|output=data-tooltip}}}}&lt;br /&gt;
&lt;br /&gt;
{{GeneEvents|{{#var:id|}}}}&lt;br /&gt;
{{HomologyList|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
[[Category:Genes]][[Category:Genes in Genome:{{#var:genome|}}]]&amp;lt;nowiki /&amp;gt;&amp;lt;/includeonly&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Template:Event&amp;diff=328</id>
		<title>Template:Event</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Template:Event&amp;diff=328"/>
				<updated>2020-06-22T19:47:42Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
&amp;lt;includeonly&amp;gt;{{#vardefine:id|{{#cleanTag:{{FULLPAGENAMEE}}|at|pre}}}}{{#vardefine:genome|{{#cleanTag:{{FULLPAGENAMEE}}|pre}}}}{{BioDB_oldid|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;nowiki /&amp;gt;{{DISPLAYTITLE:{{#var:id|}}}}{{#CustomMsg:Help:Event.ini|ini}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
''{{TypeEvent|{{PAGENAME}}}}''&amp;lt;nowiki /&amp;gt;{{BioDB_event|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
{{BioDB_event_metrics|{{#var:id}}}}&amp;lt;nowiki /&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;tablebox event-assembly&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Gene&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{#ifeq:{{#var:gene_id|}}||NA|[[Gene:{{#var:gene_id|}}@Genome:{{#var:genome|}}|{{#var:gene_id|}}]]&lt;br /&gt;
}}{{#ifeq:{{#var:gene_name|}}|||&amp;amp;nbsp;{{!}} ''{{#var:gene_name|}}'' }}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Description&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{#if:{{#var:description|}}|{{#var:description|}}|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Coordinates&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span class='genome-nor'&amp;gt;{{#var:chro_c|}}:{{#var:start_c|}}-{{#var:end_c|}}:{{#var:strand_c|}}&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-coords|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord C1 exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_c1|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord A exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_a|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Coord C2 exon&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:co_c2|}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
		&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Length&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large=8 columns&amp;quot;&amp;gt;{{#var:length_n|}} bp{{HelpLinkedPage|type=helpicon|msg=event-length|output=data-tooltip}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Sequences&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Splice sites&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-splice|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
                         {{Score_SS|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Exon sequences&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-exon|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq C1 exon&amp;lt;/div&amp;gt;{{#var:seq_c1|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq A exon&amp;lt;/div&amp;gt;{{#var:seq_a|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Seq C2 exon&amp;lt;/div&amp;gt;{{#var:seq_c2|}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;		&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;VastDB Features&amp;lt;/div&amp;gt;{{BioDB_mappability|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Vast-tools module Information&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-vastdbfeatures|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Secondary ID&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:oldid|}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-internal|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Average complexity&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:complex|}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-complexity|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Mappability confidence:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#ifeq:{{#var:minc|}}||NA|{{#var:minc|}}%={{#var:mexc1|}}={{#var:mexc2|}}%}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-mappability|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Protein Impact&amp;lt;/div&amp;gt;{{BioDB_protimpact|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;&amp;quot;&amp;gt;{{#var:protimpact|No protein impact description available}}{{HelpLinkedPage|type=helpicon|msg=event-impact|output=data-tooltip}}&lt;br /&gt;
{{PDBshow|{{#var:id|}}}}&lt;br /&gt;
                &amp;lt;/div&amp;gt;{{BioDB_protdisorder|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Features&amp;lt;/span&amp;gt;&lt;br /&gt;
&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Disorder rate:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;C1={{#var:c1dis|NA}} A={{#var:adis|NA}} C2={{#var:c2dis|NA}}&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-disorder|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
                                &amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;block&amp;quot; style=&amp;quot;display:block !important&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;body&amp;quot; style=&amp;quot;display:block !important&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;amp;nbsp;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin disorder-img&amp;quot;&amp;gt;&lt;br /&gt;
{{#BioDB:prosite_url|{{#var:id|}},DISORDER}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|DISORDER}}{{#BioDB_clear:}}&lt;br /&gt;
&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Domain overlap (PROSITE):&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&lt;br /&gt;
					&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;{{BioDB_prosite|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
						&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Info&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-prosite|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C1:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c1prosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;A:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:aprosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C2:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c2prosite|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin prosite-img&amp;quot;&amp;gt;{{#BioDB:prosite_url|{{#var:id|}},PROSITE}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|PROSITE}}{{#BioDB_clear:}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;/div&amp;gt;&lt;br /&gt;
					&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Domain overlap (PFAM):&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;&lt;br /&gt;
					&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;{{BioDB_pfam|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
						&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Info&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-pfam|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold up&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;div class=&amp;quot;body&amp;quot;&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C1:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c1pfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;A:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:apfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;C2:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:c2pfam|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
							&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin pfam-img&amp;quot;&amp;gt;{{#BioDB:prosite_url|{{#var:id|}},PFAM}}{{ExternalImgURL|{{#BioDB_value:prosite_url.URL|}}|PFAM}}{{#BioDB_clear:}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
						&amp;lt;/div&amp;gt;&lt;br /&gt;
					&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;{{BioDB_ppi|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Degree:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:degree|NA}}&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Betweeness:&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#var:betweenness|NA}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-degree|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Associated events&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{Associated|{{#var:id|}}|{{#var:genome|}}}}{{HelpLinkedPage|type=helpicon|msg=event-associated|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4&amp;quot;&amp;gt;Conservation&amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-conservation|output=data-tooltip}}{{ConservationFull|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;{{BioDB primer|{{#var:id|}}|{{#var:genome|}}}}&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Primers PCR&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;&lt;br /&gt;
		&amp;lt;div class=&amp;quot;block&amp;quot;&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;head&amp;quot;&amp;gt;&amp;lt;span&amp;gt;Suggestions for RT-PCR validation&amp;lt;/span&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-primers|output=data-tooltip}}&amp;lt;span class=&amp;quot;unfold down&amp;quot;&amp;gt;&amp;lt;/span&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;div class=&amp;quot;body folded&amp;quot;&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;F: &amp;lt;/div&amp;gt;{{#ifeq:{{#var:primerf|}}||&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;No suggested primer sequences&amp;lt;/div&amp;gt;|&amp;lt;div class=&amp;quot;contentin bioseq&amp;quot;&amp;gt;{{#var:primerf|}}&amp;lt;/div&amp;gt;}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;R: &amp;lt;/div&amp;gt;{{#ifeq:{{#var:primerr|}}||&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;No suggested primer sequences&amp;lt;/div&amp;gt;|&amp;lt;div class=&amp;quot;contentin bioseq&amp;quot;&amp;gt;{{#var:primerr|}}&amp;lt;/div&amp;gt;}}&amp;lt;/div&amp;gt;&lt;br /&gt;
				&amp;lt;div class=&amp;quot;rowin&amp;quot;&amp;gt;&amp;lt;div class=&amp;quot;labelin&amp;quot;&amp;gt;Band lengths: &amp;lt;/div&amp;gt;&amp;lt;div class=&amp;quot;contentin&amp;quot;&amp;gt;{{#ifeq:{{#var:pskipping|}}|||{{#var:pskipping|}}-{{#var:pinclusion|}}}}&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
			&amp;lt;/div&amp;gt;&lt;br /&gt;
		&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;row&amp;quot;&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;label small-6 large-4 columns&amp;quot;&amp;gt;Annotated function&amp;lt;div class=&amp;quot;submitfunction&amp;quot;&amp;gt;[[EventFunction|(Submit a function)]]&amp;lt;/div&amp;gt;&amp;lt;/div&amp;gt;&lt;br /&gt;
	&amp;lt;div class=&amp;quot;content small-6 large-8 columns&amp;quot;&amp;gt;{{AnnotatedFunction|{{#var:id|}}|{{#var:genome|}}}}&amp;lt;/div&amp;gt;		&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;br /&amp;gt;&lt;br /&gt;
====GENOMIC CONTEXT====&lt;br /&gt;
&amp;lt;div class=&amp;quot;content large-12&amp;quot;&amp;gt;&lt;br /&gt;
&amp;lt;div style=&amp;quot;float:right&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-browser|output=data-tooltip}}&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;/div&amp;gt;&lt;br /&gt;
&amp;lt;div class=&amp;quot;browser-container genome-nor&amp;quot;&amp;gt;&lt;br /&gt;
{{#embedUCSC:chrom={{#var:chro_c|}}|start={{#var:start_c|}}|end={{#var:end_c|}}|genome_id={{#var:genome|}}}}&amp;lt;/div&amp;gt;&lt;br /&gt;
====INCLUSION PATTERN====&lt;br /&gt;
&amp;lt;div class=&amp;quot;tissuevalue-list sample-chart&amp;quot;&amp;gt;{{HelpLinkedPage|type=helpicon|msg=event-tissuevalue|output=data-tooltip}}&amp;lt;/div&amp;gt;{{#printCharts:}}&lt;br /&gt;
&amp;lt;hr&amp;gt;&lt;br /&gt;
{{#specialImages:{{#var:id|}}|{{#var:genome|}}|AS_ABIOTIC,AS_BIOTIC,AS_LIGHT,AS_SPL_FACTORS|Abiotic stress,Biotic stress,Light response,RNA-processing factors|{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-abiotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-biotic|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-light|output=data-tooltip}},{{HelpLinkedPage|type=helpicon|msg=event-specialpsi-spl_factors|output=data-tooltip}}}}&lt;br /&gt;
&amp;lt;!--{{SpecialPSIDiv}}--&amp;gt;&lt;br /&gt;
{{Event Links|{{#var:genome}}|{{#var:gene_id}}|{{#var:gene_name}}}}&lt;br /&gt;
{{PDBdiv|{{#var:genome|}}}}[[Category:Events]][[Category:Events in Genome:{{#var:genome|}}]]&amp;lt;nowiki /&amp;gt;&amp;lt;/includeonly&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=327</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=327"/>
				<updated>2020-06-22T13:54:04Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: /* How should I interpret the domain information? */&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.2.2''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
&amp;quot;Domain information is currently only available for cassette exons.&amp;quot;&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=326</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=326"/>
				<updated>2020-06-22T13:53:42Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.2.2''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
&amp;quot;Domain information is currently only available for cassette exons.&amp;quot;&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=325</id>
		<title>FAQ</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=FAQ&amp;diff=325"/>
				<updated>2020-06-22T13:53:00Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the inclusion level (PSI) of a given AS event quantified? ====&lt;br /&gt;
AS event quantification is performed using [https://github.com/vastgroup/vast-tools ''vast-tools'']. ''vast-tools'' uses different modules to quantify cassette exons, microexons, alternative 5' and 3' splice sites and intron retention (reflected in the 'vast-tools module' field in the ‘VastDB Features’ section of each event). For detailed information about how the quantification works, please refer to the Supplementary Information of [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]. Current inclusion data in PastDB corresponds to ''vast-tools v2.2.2''.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What AS events are displayed in PastDB? ====&lt;br /&gt;
PastDB contains information for all AS events detected and quantified in [https://github.com/vastgroup/vast-tools ''vast-tools'']. However, only a selection of them are displayed in the UCSC track and in the Gene page. These are the events that have the higher PSI variation across samples. If you are interested in an event that is not displayed, you can directly look for it using the search box in the from page.&lt;br /&gt;
&lt;br /&gt;
==== What do the colors and block thickness in the UCSC track mean? ====&lt;br /&gt;
The colors signify the different types of AS events, whereas the block thickness inform about the type of sequence.&lt;br /&gt;
*For any individual cassette exon event (including microexons), each C1, A and C2 exons are represented. The alternative exon (A) thus corresponds to the exon in between.&lt;br /&gt;
**Blue: simple cassette exon. “Simple” is defined as cassette exons for which ≥95% of the reads used to quantify their PSI come from the three reference exon-exon junctions, which are C1A, AC2 and C1C2. It corresponds to “S” or “MIC_S” in ‘Average complexity’.&lt;br /&gt;
**Purple: cassette exon event of intermediate complexity. This is defined as those alternative exons for which ≥50% and ≤95% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C1” or “C2” in ‘Average complexity’.&lt;br /&gt;
**Red: complex cassette exon event, for which &amp;lt;50% of the reads used to quantify their PSI come from the three reference exon-exon junctions. Corresponds to “C3”, “ME” or “MIC_M” in ‘Average complexity’.&lt;br /&gt;
**Black: groups multiple neighboring cassette exon events. Black tracks are only informative and do not link to any page in VASTDB.&lt;br /&gt;
&lt;br /&gt;
*For Intron Retention events: Orange track. Thick blocks correspond to the intronic sequence, and the thin blocks to the adjoining exons (C1 and C2).&lt;br /&gt;
&lt;br /&gt;
*For Alternative 3' and 5' splice site choice event: Dark Green and Light Green, respectively. In both cases, thick block corresponds to the alternative sequence, whereas the thin blocks are the constant exonic sequences (C1 and C2). For these events, at least two tracks are shown: for sequence exclusion (the most internal splice site; EventID-1/N) and for sequence inclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the splice site scores calculated? ====&lt;br /&gt;
These scores were calculated using score5.pl and score3.pl from  [http://www.ncbi.nlm.nih.gov/pubmed/15285897 Yeo and Burge, 2004] . This method uses a position weight matrix and calculates deviation from the consensus. For 5’ splice sites, three exonic and six intronic positions surrounding the exon-intron junction were analyzed, and for the 3’ splice sites, 20 intronic and 3 exonic positions were analyzed.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How is the impact on the ORF predicted? ====&lt;br /&gt;
The pipeline to predict ORF impact is described in [https://www.ncbi.nlm.nih.gov/pubmed/25525873 Irimia ''et al.'', 2014]. Several things must be kept in mind when using this information as is:&lt;br /&gt;
* The prediction is based on the impact that the specific alternative sequence is likely to have when included or excluded from the transcript in isolation. That is, if there are other associated AS events (e.g. mutually exclusive or coordinated exons) the prediction may not be accurate. &lt;br /&gt;
* We keep improving and polishing these annotations, and new versions are often released.  Make sure you use the most up-to-date version.&lt;br /&gt;
* Like any other prediction, our annotations may be inaccurate. Please check your results carefully and, as with any other dataset in PastDB, use at your own risk.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How should I interpret the domain information? ====&lt;br /&gt;
&amp;quot;Domain information is currently only available for cassette exons.&amp;quot;&lt;br /&gt;
When an exon (either C1, A or C2) overlap a PROSITE or PFAM domain, it shows the following information:&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&amp;lt;div align=&amp;quot;center&amp;quot;&amp;gt;''Dom_ID'' = ''Dom_Name'' = ''Type_Overlap''(''%Dom_Overlap'' = ''%Exon_Overlap'')&amp;lt;/div&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
The meaning of each field is explained below:&lt;br /&gt;
*''Dom_ID'': Domain ID in either PROSITE or PFAM databases. For PROSITE, domains with ID P0* (high frequency motifs) are excluded.&lt;br /&gt;
*''Dom_Name'': Domain name as provided by PROSITE or PFAM databases.&lt;br /&gt;
*''Type_Overlap'': There are four possible ways in which an exon can overlap a protein domain:&lt;br /&gt;
**The whole exonic sequence fully overlaps with a domain (FE, Full Exon).&lt;br /&gt;
**The whole domain is fully encoded within an exon (WD, Whole Domain).&lt;br /&gt;
**The upstream (5') of the exon overlaps the domain (PU, Partial Upstream).&lt;br /&gt;
**The downstream (3') of the exon overlaps the domain (PD, Partial Downstream).&lt;br /&gt;
*''%Dom_overlap'': percent of the domain encode by the exon.&lt;br /&gt;
*''%Exon_overlap'': percent of the exon that overlaps the domain.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== How are the primers for RT-PCR validation designed? ====&lt;br /&gt;
Primers are designed automatically using Primer3 (optimal primer lenght = 21 nt; optimal Tm = 61 ºC). As a general rule, primers are located in the C1 and C2 exonic sequences, so two RT-PCR products will be produced: a shorter one (from C1 to C2, skipping the A sequence) and a longer one (including the A sequence). This is provided in ‘Band lengths’. &lt;br /&gt;
To minimize PCR amplification bias towards shorter amplicons (i.e. over-representation of the skipping form) and, at the same time, optimize the visualization in agarose gels, primers are designed based on the size relationship between the two predicted amplicons. This is based on the following rules:&lt;br /&gt;
*Alternative sequence LE &amp;lt; 15 nt =&amp;gt; optimal skipping band size = 100 nt.&lt;br /&gt;
*Alternative sequence 15 ≤ LE &amp;lt; 25 nt =&amp;gt; optimal skipping band size = 110 nt.&lt;br /&gt;
*Alternative sequence 25 ≤ LE &amp;lt; 40 nt =&amp;gt; optimal skipping band size = 120 nt.&lt;br /&gt;
*Alternative sequence 40 ≤ LE &amp;lt; 65 nt =&amp;gt; optimal skipping band size = 140 nt.&lt;br /&gt;
*Alternative sequence 65 ≤ LE &amp;lt; 100 nt =&amp;gt; optimal skipping band size = 175 nt.&lt;br /&gt;
*Alternative sequence 100 ≤ LE &amp;lt; 200 nt =&amp;gt; optimal skipping band size = 250 nt.&lt;br /&gt;
*Alternative sequence 200 ≤ LE &amp;lt; 300 nt =&amp;gt; optimal skipping band size = 300 nt.&lt;br /&gt;
*Alternative sequence 300 ≤ LE &amp;lt; 1000 nt =&amp;gt; optimal skipping band size = 350 nt.&lt;br /&gt;
*Alternative sequence LE &amp;gt; 1000 nt =&amp;gt; primers not designed. A three-primer strategy is recommended.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== What are the quality scores (QC) in the PSI plots? ====&lt;br /&gt;
As provided by ''vast-tools''; from the README: Quality scores, and number of corrected inclusion and exclusion reads (qual@inc,exc):&lt;br /&gt;
*Score 1: Read coverage, based on actual reads (as used in [http://www.cell.com/abstract/S0092-8674(14)01512-8 Irimia et al., ''Cell'' 2014]:&lt;br /&gt;
**For EX: OK/LOW/VLOW: (i) ≥20/15/10 actual reads (i.e. before mappability correction) mapping to all exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two groups of inclusion splice junctions (upstream or downstream the alternative exon), and ≥15/10/5 to the other group of inclusion splice junctions.&lt;br /&gt;
**For EX (microexon module): OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of exclusion splice junctions, OR (ii) ≥20/15/10 actual reads mapping to the sum of inclusion splice junctions.&lt;br /&gt;
**For INT: OK/LOW/VLOW: (i) ≥20/15/10 actual reads mapping to the sum of skipping splice junctions, OR (ii) ≥20/15/10 actual reads mapping to one of the two inclusion exon-intron junctions (the 5' or 3' of the intron), and ≥15/10/5 to the other inclusion splice junctions.&lt;br /&gt;
**For ALTD and ALTA: OK/LOW/VLOW: (i) ≥40/20/10 actual reads mapping to the sum of all splice junctions involved in the specific event.&lt;br /&gt;
**For any type of event: SOK: same thresholds as OK, but a total number of reads ≥100.&lt;br /&gt;
**For any type of event: N: does not meet the minimum threshold (VLOW).&lt;br /&gt;
*Score 2: Read coverage, based on corrected reads (similar values as per Score 1).&lt;br /&gt;
*Score 3: Read coverage, based on uncorrected reads mapping only to the reference C1A, AC2 or C1C2 splice junctions (similar values as per Score 1). Always NA for intron retention events.&lt;br /&gt;
*Score 4: Imbalance of reads mapping to inclusion splice junctions (only for exon skipping events quantified by the splice site-based or transcript-based modules; For intron retention events, numbers of reads mapping to the upstream exon-intron junction, downstream intron-exon junction, and exon-exon junction in the format A=B=C)&lt;br /&gt;
**OK: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;lt; 2.&lt;br /&gt;
**B1: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 2 but &amp;lt; 5.&lt;br /&gt;
**B2: the ratio between the total number of reads supporting inclusion for splice junctions upstream and downstream the alternative exon is &amp;gt; 5.&lt;br /&gt;
**Bl/Bn: low/no read coverage for splice junctions supporting inclusion.&lt;br /&gt;
*Score 5: Complexity of the event (only for exon skipping events quantified by the splice site-based or transcript-based modules); For intron retention events, p-value of a binomial test of balance between reads mapping to the upstream and downstream exon-intron junctions, modified by reads mapping to a 200-bp window in the centre of the intron (see [http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 Braunschweig et al., 2014]).&lt;br /&gt;
**S: percent of complex reads (i.e. those inclusion- and exclusion-supporting reads that do not map to the reference C1A, AC2 or C1C2 splice junctions) is &amp;lt; 5%.&lt;br /&gt;
**C1: percent of complex reads is &amp;gt; 5% but &amp;lt; 20%.&lt;br /&gt;
**C2: percent of complex reads is &amp;gt; 20% but &amp;lt; 50%.&lt;br /&gt;
**C3: percent of complex reads is &amp;gt; 50%.&lt;br /&gt;
**NA: low coverage event.&lt;br /&gt;
*inc,exc: total number of reads, corrected for mappability, supporting inclusion and exclusion.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
==== Where does the PastDB logo come from?  ====&lt;br /&gt;
The image depicts a pair of alternative splice acceptor sites (yellow) as the bridge between a seedling and a mature plant, representing plant development.  The image is an original design by Yamile Márquez.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Publications&amp;diff=324</id>
		<title>Publications</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Publications&amp;diff=324"/>
				<updated>2020-06-22T13:44:53Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;__NOTOC__&lt;br /&gt;
&lt;br /&gt;
====  PastDB publication ====&lt;br /&gt;
* Martin, G., Marquez, Y., Duque, P., Irimia, M. (2020). Alternative splicing landscapes in Arabidopsis thaliana across tissues and stress conditions reveal major differences with animals. In preparation.&lt;br /&gt;
&lt;br /&gt;
====  VastDB publication (v1.0) ====&lt;br /&gt;
* Tapial, J., Ha, K. C. H., Sterne-Weiler, T., Gohr, A., Braunschweig, U., Hermoso-Pulido, A., Quesnel-Vallières, M., Permanyer, J., Sodaei, R., Marquez, Y., Cozzuto, L., Wang, X., Gómez-Velázquez, M., Rayon, T., Manzanares, M., Ponomarenko, J., Blencowe, B. J., Irimia, M. (2017). An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms. ''Genome Research, 27''(10), 1759–1768. [[http://genome.cshlp.org/content/27/10/1759.long link]] [[https://www.ncbi.nlm.nih.gov/pubmed/28855263 PubMed]]&lt;br /&gt;
&lt;br /&gt;
==== vast-tools  ====&lt;br /&gt;
* Tapial, J., Ha, K. C. H., Sterne-Weiler, T., Gohr, A., Braunschweig, U., Hermoso-Pulido, A., Quesnel-Vallières, M., Permanyer, J., Sodaei, R., Marquez, Y., Cozzuto, L., Wang, X., Gómez-Velázquez, M., Rayon, T., Manzanares, M., Ponomarenko, J., Blencowe, B. J., Irimia, M. (2017). An atlas of alternative splicing profiles and functional associations reveals new regulatory programs and genes that simultaneously express multiple major isoforms. ''Genome Research, 27''(10), 1759–1768. [[http://genome.cshlp.org/content/27/10/1759.long link]] [[https://www.ncbi.nlm.nih.gov/pubmed/28855263 PubMed]]&lt;br /&gt;
&lt;br /&gt;
* Irimia, M., Weatheritt, R.J., Ellis, J., Parikshak, N.N., Gonatopoulos-Pournatzis, T., Babor, M., Quesnel-Vallières, M., Tapial, J., Raj, B., O’Hanlon, D., Barrios-Rodiles, M., Sternberg, M.J.E., Cordes, S.P., Roth, F.P., Wrana, J.L., Geschwind, D.H., Blencowe, B.J. (2014). A highly conserved program of neuronal microexons is misregulated in autistic brains. ''Cell'', 59:1511-23. [[http://www.cell.com/abstract/S0092-8674(14)01512-8 link]] [[http://www.ncbi.nlm.nih.gov/pubmed/25525873 PubMed]]&lt;br /&gt;
&lt;br /&gt;
==== Intron retention analysis ====&lt;br /&gt;
* Braunschweig, U., Barbosa-Morais, N.L., Pan, Q., Nachman, E., Alipahani, B., Gonatopoulos-Pournatzis, T., Frey, B., Irimia, M., Blencowe, B.J. (2014). Widespread intron retention in mammals functionally tunes transcriptomes. ''Genome Research'', 24:1774-86. [[http://genome.cshlp.org/content/early/2014/09/24/gr.177790.114 link]] [[http://www.ncbi.nlm.nih.gov/pubmed/25258385 PubMed]]&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=323</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=323"/>
				<updated>2020-06-22T13:40:15Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
&lt;br /&gt;
====&amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages.&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_IMPACT-araTha10-v2.3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v2.3.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=322</id>
		<title>Downloads</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=Downloads&amp;diff=322"/>
				<updated>2020-06-22T13:39:14Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;From this page you can download tables with the information in PastDB. Tables with different features of the database can be downloaded separately:&lt;br /&gt;
====Arabidopsis thaliana====&lt;br /&gt;
=====AS events=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EVENT_INFO-araTha10.tab.gz EVENTS table]  - Information about AS event coordinates and sequences. TAIR10 asssembly.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PSI_TABLE-araTha10.tab.gz PSI table] - Inclusion patterns of AS events across tissues, cell types and developmental stages.&lt;br /&gt;
=====Event features=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/SPLICE_SITE_SCORES-araTha10.tab.gz SPLICE SITES table] - Sequences and strength scores of 5' and 3' splice sites of alternative exons.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PCR_PRIMERS-araTha10.tab.gz PCR VALIDATION table] - Suggested primer sequences and expected band lengths for validation of AS events by RT-PCR.&lt;br /&gt;
=====Protein impact=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_IMPACT-araTha10-v2.3.tab.gz PROTEIN IMPACT table] - Effect of the AS event in the open reading frame of the transcript. Version v2.3.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_ISOFORMS-araTha10.tab.gz PROTEIN ISOFORMS] -  Mappings of events to ProteinIDs.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_PFAM-araTha10.tab.gz DOMAINS table (PFAM)] -  Mappings to Pfam domains&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_PROSITE-araTha10.tab.gz DOMAINS table (PROSITE)] - Mappings to PROSITE domains.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/PROT_DISORDER-araTha10.tab.gz PROTEIN DISORDERED REGIONS table] - Intrinsic disorder rates for A, C1 and C2 exons, using disopred3.&lt;br /&gt;
=====Genes=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/GENE_INFO-araTha10.tab.gz GENES table] - Information about gene names, descriptions, genomic coordinates and biotypes.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EXPRESSION_TABLE-araTha10.tab.gz EXPRESSION table] - Gene expression across tissues, cell types and developmental stages. Measured in cRPKM and in raw reads.&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/EVENTID_to_GENEID-araTha10.tab.gz GENE-EVENTS table] - Table relating genes to AS events.&lt;br /&gt;
=====Samples=====&lt;br /&gt;
* [{{SERVER}}/downloads/araTha10/SAMPLE_INFO-araTha10.tab.gz SAMPLE_INFO table] - SRA identifiers and other information related to RNA-seq data used in this database.&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=About&amp;diff=321</id>
		<title>About</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=About&amp;diff=321"/>
				<updated>2020-06-22T11:48:02Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;PastDB is a database of Alternative Splicing (AS) profiles across multiple tissues and environmental conditions of &amp;lt;i&amp;gt;Arabidopsis thaliana&amp;lt;/i&amp;gt;. PastDB contains AS events (including exon skipping, alternative 5' and 3' splice sites and retained introns). AS event identification and sequence inclusion level quantification in RNA-seq samples have been performed with [https://github.com/vastgroup/vast-tools VAST-TOOLS].&lt;br /&gt;
&lt;br /&gt;
In addition to AS inclusion levels, PastDB provides general information about the AS events, including genomic and sequence context, impact on the reading frame, overlap with protein domains and disordered regions and primers for AS event validation through RT-PCR. Moreover, it also provides measures of Gene Expression, using the cRPKM metric.&lt;br /&gt;
&lt;br /&gt;
If you see an AS event that you find inconsistent, or you have any questions, comments or suggestions about the database, please do not hesitate to e-mail us to [mailto:vastdb@googlegroups.com vastdb@googlegroups.com].&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=About&amp;diff=320</id>
		<title>About</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=About&amp;diff=320"/>
				<updated>2020-06-22T11:46:36Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;PastDB is a database of Alternative Splicing (AS) profiles across multiple tissues and environmental conditions of Arabidopsis thaliana. PastDB contains AS events (including exon skipping, alternative 5' and 3' splice sites and retained introns). AS event identification and sequence inclusion level quantification in RNA-seq samples have been performed with [https://github.com/vastgroup/vast-tools VAST-TOOLS].&lt;br /&gt;
&lt;br /&gt;
In addition to AS inclusion levels, PastDB provides general information about the AS events, including genomic and sequence context, impact on the reading frame, overlap with protein domains and disordered regions and primers for AS event validation through RT-PCR. Moreover, it also provides measures of Gene Expression, using the cRPKM metric.&lt;br /&gt;
&lt;br /&gt;
If you see an AS event that you find inconsistent, or you have any questions, comments or suggestions about the database, please do not hesitate to e-mail us to [mailto:vastdb@googlegroups.com vastdb@googlegroups.com].&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	<entry>
		<id>http://pastdb.crg.eu/w/index.php?title=EventFunction&amp;diff=319</id>
		<title>EventFunction</title>
		<link rel="alternate" type="text/html" href="http://pastdb.crg.eu/w/index.php?title=EventFunction&amp;diff=319"/>
				<updated>2020-06-22T11:44:45Z</updated>
		
		<summary type="html">&lt;p&gt;Mirimia: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;{{NAMESPACE}}&lt;br /&gt;
==Submit functional annotations for AS events==&lt;br /&gt;
&lt;br /&gt;
Dear PastDB user,&lt;br /&gt;
&lt;br /&gt;
Our goal is to make PastDB (and VastDB) a comprehensive resource for the research community, gathering information about the behaviour of alternative splicing events at many different levels, and displaying it in a concise and intuitive manner. With that in mind, we think that displaying brief annotations of the biological functions described for some of our AS events, together with links to bibliographical evidence, could be a very useful feature for future PastDB releases. &lt;br /&gt;
&lt;br /&gt;
That's why we kindly ask for your help. If you have published references speaking about the effects of an AS event with a ''vast-tools'' ID, you can let us know using this form, and we will include it in our next release, so that other researchers can benefit of your knowledge too.&lt;br /&gt;
&lt;br /&gt;
Thank you very much in advance,&lt;br /&gt;
&lt;br /&gt;
The VastDB/PastDB team&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
P.S. If you have many annotations, you can also send us a tab-delimited text file to [mailto:vastdb@googlegroups.com vastdb@googlegroups.com], and we will add it to our dataset.&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
&amp;lt;emailform&amp;gt;&lt;br /&gt;
 {| &lt;br /&gt;
 | Name: || &amp;lt;emailform name=40 /&amp;gt; ||&lt;br /&gt;
 |-&lt;br /&gt;
 | Email: || &amp;lt;emailform from=40 /&amp;gt; ||&lt;br /&gt;
 |- &lt;br /&gt;
 | Event ID: || &amp;lt;emailform event=40 /&amp;gt; || ''(e.g. MmuEX0025260)''&lt;br /&gt;
 |-&lt;br /&gt;
 | PubMed ID: || &amp;lt;emailform pmid=40 /&amp;gt; || ''(e.g. [https://www.ncbi.nlm.nih.gov/pubmed/20164337 20164337])''&lt;br /&gt;
 |-&lt;br /&gt;
 | Annotation: || &amp;lt;emailform function=60x8 /&amp;gt; || ''(e.g. LSD1 isoforms display in vitro a comparable demethylase activity, yet the inclusion of exon E8a (MmuEX0025260) reduces LSD1 repressor activity on a reporter gene. The knockdown of neurospecific variants in cortical neurons results in the inhibition of neurite maturation, whereas overexpression of the same variants enhances it. Instead, perturbation of LSD1 isoforms that are devoid of the neurospecific exon elicits no morphogenic effect.)''&lt;br /&gt;
 |-&lt;br /&gt;
 ||  || &amp;lt;emailform submit=&amp;quot;Submit Annotation&amp;quot; /&amp;gt; ||&lt;br /&gt;
 |}&lt;br /&gt;
 &amp;lt;/emailform&amp;gt;&lt;br /&gt;
 &amp;lt;emailform result&amp;gt;&lt;br /&gt;
Thank you for your contribution!&lt;br /&gt;
&lt;br /&gt;
Our data curation team will review this to include it in the next PastDB release.&lt;br /&gt;
 {| width=&amp;quot;300px&amp;quot;&lt;br /&gt;
 | '''Name:''' &amp;lt;emailform name /&amp;gt;&lt;br /&gt;
 | '''Email:''' &amp;lt;emailform from/&amp;gt;&lt;br /&gt;
 | '''Event ID:''' &amp;lt;emailform event /&amp;gt;&lt;br /&gt;
 | '''PMID:''' &amp;lt;emailform pmid /&amp;gt;&lt;br /&gt;
 | '''Biological function:''' &amp;lt;emailform function /&amp;gt;&lt;br /&gt;
 |}&lt;br /&gt;
 &amp;lt;/emailform&amp;gt;&lt;/div&gt;</summary>
		<author><name>Mirimia</name></author>	</entry>

	</feed>