<?xml version='1.0'?><rss version="2.0" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:georss="http://www.georss.org/georss" xmlns:atom="http://www.w3.org/2005/Atom" >
<channel>
	<title><![CDATA[BOL: Create random 1000 INDEL in genome !]]></title>
	<link>https://bioinformaticsonline.com/snippets/view/42592/create-random-1000-indel-in-genome?</link>
	<atom:link href="https://bioinformaticsonline.com/snippets/view/42592/create-random-1000-indel-in-genome?" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
	<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/snippets/view/42592/create-random-1000-indel-in-genome</guid>
	<pubDate>Sun, 10 Jan 2021 09:15:26 -0600</pubDate>
	<link>https://bioinformaticsonline.com/snippets/view/42592/create-random-1000-indel-in-genome</link>
	<title><![CDATA[Create random 1000 INDEL in genome !]]></title>
	<description><![CDATA[<code>(base) ➜  dupStudy git:(master) ✗ perl ../simuG.pl -refseq simuSNP.simseq.genome.fa -indel_count 1000 -prefix simuINDEL

[Sun Jan 10 16:14:00 2021]
Starting simuG ..

[Sun Jan 10 16:14:00 2021]
Check specified options ..
Running simuG for SNP/INDEL simulation &gt;&gt;
Ignore all options for CNV/inversion/translocation simulation.

This simulation use the random seed: 1678440514

The option indel_count has been specified: indel_count = 1000
The option ins_del_ratio has been specified: ins_del_ratio = 1
The option indel_size_powerlaw_alpha has been specified: indel_size_powerlaw_alpha = 2
The option indel_size_powerlaw_constant has been specified: indel_size_powerlaw_constant = 0.5

[Sun Jan 10 16:14:00 2021]
Introducing random INDELs based on the following parameters:
&gt; indel_count = 1000
&gt; ins_del_ratio = 1
&gt; indel_size_powerlaw_alpha = 2
&gt; indel_size_powerlaw_constant = 0.5

[Sun Jan 10 16:14:00 2021]
Simulation completed! :)

[Sun Jan 10 16:14:00 2021]
Generating output files ..

Generating the correspondance map for genomic variants introduced during simulation:
simuINDEL.refseq2simseq.map.txt

Generating reference-based vcf file for genomic variants introduced during simulation:
simuINDEL.refseq2simseq.INDEL.vcf

[Sun Jan 10 16:14:00 2021]
Done! :)</code>]]></description>
	<dc:creator>Jit</dc:creator>
</item>

</channel>
</rss>