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	<title><![CDATA[BOL: SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/view/36616/srbreak-a-read-depth-and-split-read-framework-to-identify-breakpoints-of-different-events-inside-simple-copy-number-variable-regions?</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/36616/srbreak-a-read-depth-and-split-read-framework-to-identify-breakpoints-of-different-events-inside-simple-copy-number-variable-regions</guid>
	<pubDate>Tue, 15 May 2018 04:42:11 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/36616/srbreak-a-read-depth-and-split-read-framework-to-identify-breakpoints-of-different-events-inside-simple-copy-number-variable-regions</link>
	<title><![CDATA[SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions]]></title>
	<description><![CDATA[SRBreak is a read-depth and split-read package written in R for identifying copy-number variants in next-generation sequencing datasets.

Note: SBReak was designed to work for multiple samples. It can work for &gt;= 2 samples, but we suggest that users should use &gt;= 5 samples as in the work tested in our paper.<p>Address of the bookmark: <a href="https://github.com/hoangtn/SRBreak" rel="nofollow">https://github.com/hoangtn/SRBreak</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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