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	<id>https://info.gersteinlab.org/index.php?action=history&amp;feed=atom&amp;title=ACT</id>
	<title>ACT - Revision history</title>
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	<updated>2026-05-12T14:40:30Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://info.gersteinlab.org/index.php?title=ACT&amp;diff=58&amp;oldid=prev</id>
		<title>Infoadmin: Created page with &#039;=== ACT === http://ACT.Gersteinlab.org was developed by Robert Bjornson &lt;robert.bjornson@yale.edu&gt;, Joel Rozowsky, Justin Jee, and others at the Gerstein Lab at Yale.  This code …&#039;</title>
		<link rel="alternate" type="text/html" href="https://info.gersteinlab.org/index.php?title=ACT&amp;diff=58&amp;oldid=prev"/>
		<updated>2010-06-09T12:01:36Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;#039;=== ACT === http://ACT.Gersteinlab.org was developed by Robert Bjornson &amp;lt;robert.bjornson@yale.edu&amp;gt;, Joel Rozowsky, Justin Jee, and others at the Gerstein Lab at Yale.  This code …&amp;#039;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;=== ACT ===&lt;br /&gt;
http://ACT.Gersteinlab.org was developed by Robert Bjornson &amp;lt;robert.bjornson@yale.edu&amp;gt;, Joel Rozowsky, Justin Jee, and others at the Gerstein Lab at Yale.&lt;br /&gt;
&lt;br /&gt;
This code takes an annotation file and one or more signal files, and computes a histogram of the &lt;br /&gt;
aggregated signal intensity around the annotations.  &lt;br /&gt;
&lt;br /&gt;
The annotations should specify an interval on the genome and a &lt;br /&gt;
strand (direction).  The aggregation will be centered around the &amp;quot;beginning&amp;quot; of the annotation, i.e. the 5&amp;#039; end&lt;br /&gt;
for + strand annotations and the 3&amp;#039; end for - annotations, and oriented as the strand.  &lt;br /&gt;
&lt;br /&gt;
Basically, the program lays a set of bins around each annotation, calculates the mean or median signal level in &lt;br /&gt;
each bin.  The final result is the accumulated data for all annotations.  &lt;br /&gt;
&lt;br /&gt;
The bins can be laid out in two ways:&lt;br /&gt;
1) Fixed size bins.  2*nbins bins, each of length radius/nbins.  &lt;br /&gt;
2) A fixed number (mbins) of bins of variable size over the annotation proper, with nbins on each size of the annotation.&lt;br /&gt;
 &lt;br /&gt;
&lt;br /&gt;
In the case of snps, we use a binary signal file, with two entries per snp:&lt;br /&gt;
&lt;br /&gt;
SNPloc      1&lt;br /&gt;
 &lt;br /&gt;
(SNPloc+1)  0&lt;br /&gt;
&lt;br /&gt;
==== Figure Legends ====&lt;br /&gt;
The figures below show the SNP density upstream and downstream of transcription start (TSS) and end site (TSE)respectively.&lt;br /&gt;
The X- axis shows the relative offset in base-pairs with respect to TSS/TSE. The plot to the left of the origin corresponds to the SNP density&lt;br /&gt;
upstream of TSS and to the rightof the origin corresponds to SNP density downstream of TES. &lt;br /&gt;
&lt;br /&gt;
These plots were made based on SNPs mapped to GENCODE annotations(GENCODEver2b).&lt;br /&gt;
These can be obtained from&lt;br /&gt;
[http://homes.gersteinlab.org/people/suganthi/outbox/rob/for-wiki/gencode_data.rel2b.gtf.gz Gencode Release 2B]&lt;br /&gt;
&lt;br /&gt;
SNPs are the SNP calls made by Richard Durbin&amp;#039;s group and is based on the files obtained from&lt;br /&gt;
[ftp://ftp.sanger.ac.uk/pub/1000genomes/REL-0907 ftp://ftp.sanger.ac.uk/pub/1000genomes/REL-0907]&lt;br /&gt;
&lt;br /&gt;
Only high quality SNPs have been used for this calculation (please check the README file that defines the criteria for a high quality SNP).&lt;br /&gt;
&lt;br /&gt;
==== ACT 2500bp ====&lt;br /&gt;
[[Image:Act-2500bp-1.jpg]]&lt;br /&gt;
&lt;br /&gt;
==== ACT 5000bp ====&lt;br /&gt;
[[Image:Act-5000bp-1.jpg]]&lt;/div&gt;</summary>
		<author><name>Infoadmin</name></author>
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