<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[Faster NGS Duplicate Marking]]></title><description><![CDATA[<p dir="auto"><a href="https://medium.com/grail-eng/faster-ngs-duplicate-marking-d7a1fd287f46" rel="nofollow ugc">https://medium.com/grail-eng/faster-ngs-duplicate-marking-d7a1fd287f46</a><br />
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<p dir="auto">Picard¹ and Sambamba 的算法类似<br />
SAMTools (rmdup)</p>
]]></description><link>http://an.forum.genostack.com/topic/637/faster-ngs-duplicate-marking</link><generator>RSS for Node</generator><lastBuildDate>Sat, 13 Jun 2026 09:22:21 GMT</lastBuildDate><atom:link href="http://an.forum.genostack.com/topic/637.rss" rel="self" type="application/rss+xml"/><pubDate>Mon, 09 May 2022 08:52:37 GMT</pubDate><ttl>60</ttl><item><title><![CDATA[Reply to Faster NGS Duplicate Marking on Mon, 09 May 2022 08:53:32 GMT]]></title><description><![CDATA[<p dir="auto"><a href="https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-016-1097-3#:~:text=PCR%20duplicates%20are%20sequence%20reads,duplicates%20appear%20proportionately%20more%20often" rel="nofollow ugc">https://bmcbioinformatics.biomedcentral.com/articles/10.1186/s12859-016-1097-3#:~:text=PCR duplicates are sequence reads,duplicates appear proportionately more often</a><br />
这个文章说去重对后面的variant call 结果影响不大  但是这样能明显减少分析的数据量</p>
]]></description><link>http://an.forum.genostack.com/post/1461</link><guid isPermaLink="true">http://an.forum.genostack.com/post/1461</guid><dc:creator><![CDATA[anneng]]></dc:creator><pubDate>Mon, 09 May 2022 08:53:32 GMT</pubDate></item></channel></rss>