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		<id>http://gtc.wi.mit.edu/index.php?action=history&amp;feed=atom&amp;title=ELANDV1</id>
		<title>ELANDV1 - Revision history</title>
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		<updated>2026-04-08T04:12:08Z</updated>
		<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>http://gtc.wi.mit.edu/index.php?title=ELANDV1&amp;diff=17880&amp;oldid=prev</id>
		<title>Sgupta at 15:06, 6 October 2009</title>
		<link rel="alternate" type="text/html" href="http://gtc.wi.mit.edu/index.php?title=ELANDV1&amp;diff=17880&amp;oldid=prev"/>
				<updated>2009-10-06T15:06:38Z</updated>
		
		<summary type="html">&lt;p&gt;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&lt;br /&gt;
== To run the program ==&lt;br /&gt;
&lt;br /&gt;
Step 1: Please copy the script titled - &amp;quot;run_eland_v1.pl&amp;quot; - from &amp;quot;\\Gobo\wicmt_public\public_apps\ELAND&amp;quot; folder to your home directory.&lt;br /&gt;
&lt;br /&gt;
Step 2: Copy the *_sequence.txt files from the &amp;quot;quality score&amp;quot; folders to your working directory where you have write permissions.&lt;br /&gt;
&lt;br /&gt;
Step 3: Open the &amp;quot;run_eland_v1.pl&amp;quot; in any text editor and modify the parameter according to the instructions in the file. Please email Sumeet Gupta, sgupta@wi.mit.edu, if you have any questions.&lt;br /&gt;
&lt;br /&gt;
Step 4: Logon to your tak account.&lt;br /&gt;
&lt;br /&gt;
Step 5: Run the perl script &amp;quot;run_eland_v1.pl&amp;quot;.&lt;br /&gt;
&lt;br /&gt;
== Output Files ==&lt;br /&gt;
&lt;br /&gt;
1. [Prefix]_[GenomeUsed]_[SeedUsed]_eland_extended.txt - Gives all the positions a read maps, if it matches to less than 10 positions.&lt;br /&gt;
&lt;br /&gt;
2. [Prefix]_[GenomeUsed]_[SeedUsed]_export.txt - Contains all read, quality value and alignment information for a lane of data.&lt;br /&gt;
&lt;br /&gt;
3. [Prefix]_[GenomeUsed]_[SeedUsed].ylf - (Y)oung (L)ab (F)ormat files - These are used as input for the young lab error model for ChIP-Seq analysis.&lt;br /&gt;
&lt;br /&gt;
4. [Prefix]_[GenomeUsed]_[SeedUsed]_sorted.txt - Contains all the uniquely mapped reads, sorted based on the position on the genome.&lt;br /&gt;
&lt;br /&gt;
5. [Prefix]_[GenomeUsed]_[SeedUsed]_genomesize.xml - Summary for the genome being used for the alignment&lt;br /&gt;
&lt;br /&gt;
6. TechnicalAnalysis-[Prefix]_[GenomeUsed]_[SeedUsed].xls - QC Report for the ELAND alignment - Please refer here for details - http://jura.wi.mit.edu/genomecorewiki/index.php/QCOutputFormat&lt;br /&gt;
&lt;br /&gt;
7. [Prefix]_[GenomeUsed]_[SeedUsed]_tagcount.txt - Gives a count for all the reads, their corresponding counts, position on the genome and the gene name if it is in the transcribed region.&lt;/div&gt;</summary>
		<author><name>Sgupta</name></author>	</entry>

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