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	<title><![CDATA[BOL: Related items]]></title>
	<link>https://bioinformaticsonline.com/related/34925?offset=530</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40510/reps-repeat-masked-phrap-with-scaffolding-a-wgs-sequence-assembler</guid>
	<pubDate>Sat, 04 Jan 2020 01:08:09 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40510/reps-repeat-masked-phrap-with-scaffolding-a-wgs-sequence-assembler</link>
	<title><![CDATA[RePS: Repeat-masked Phrap with scaffolding, a WGS sequence assembler]]></title>
	<description><![CDATA[<p>RePS (Repeat-masked Phrap with scaffolding), a WGS sequence assembler, that explicitly identifies exact kmer repeats from the shotgun data and removes them prior to the assembly. The established software Phrap is used to compute meaningful error probabilities for each base. Clone-end-pairing information is used to construct scaffolds that order and orient the contigs. The updated version of RePS incorporates some of the ideas introduced by Phusion on clustering</p>
<p><img src="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC186573/bin/45793-17f1_F4TT.jpg" alt="image" style="border: 0px;"></p>
<p>More at</p>
<p><a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC186573/">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC186573/</a></p><p>Address of the bookmark: <a href="ftp://ftp.genomics.org.cn/pub/ricedb/Tools/RePS/RePS-IBM-AIX.tar.gz" rel="nofollow">ftp://ftp.genomics.org.cn/pub/ricedb/Tools/RePS/RePS-IBM-AIX.tar.gz</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
</item>
<item>
	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/42310/dada2-fast-and-accurate-sample-inference-from-amplicon-data-with-single-nucleotide-resolution</guid>
	<pubDate>Tue, 10 Nov 2020 20:26:00 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/42310/dada2-fast-and-accurate-sample-inference-from-amplicon-data-with-single-nucleotide-resolution</link>
	<title><![CDATA[DADA2: Fast and accurate sample inference from amplicon data with single-nucleotide resolution]]></title>
	<description><![CDATA[<p>The&nbsp;<a href="https://benjjneb.github.io/dada2/tutorial.html">DADA2 tutorial</a>&nbsp;goes through a typical workflow for paired end Illumina Miseq data: raw amplicon sequencing data is processed into the table of exact&nbsp;<strong>amplicon sequence variants (ASVs)</strong>&nbsp;present in each sample.</p>
<p>The&nbsp;<a href="https://benjjneb.github.io/dada2/bigdata.html">DADA2 Workflow on Big Data</a>&nbsp;goes through workflow optimized to run on large datasets (10s of millions to billions of reads).</p>
<p>An&nbsp;<a href="https://benjjneb.github.io/dada2/ITS_workflow.html">ITS-specific version of the DADA2 workflow</a>&nbsp;identifies and verifiably removes primers on both ends of each ITS read, a key step due to the variable length of the ITS region.</p>
<p>Short demonstrations of&nbsp;<a href="https://benjjneb.github.io/dada2/assign.html">assigning taxonomy</a>&nbsp;and&nbsp;<a href="https://benjjneb.github.io/dada2/assign.html">assigning species</a>&nbsp;to sequences.</p><p>Address of the bookmark: <a href="https://benjjneb.github.io/dada2/index.html" rel="nofollow">https://benjjneb.github.io/dada2/index.html</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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