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	<title><![CDATA[BOL: VG: variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods?</link>
	<atom:link href="https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods?" rel="self" type="application/rss+xml" />
	<description><![CDATA[]]></description>
	
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods</guid>
	<pubDate>Tue, 28 Jan 2020 03:53:24 -0600</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/40711/vg-variation-graph-data-structures-interchange-formats-alignment-genotyping-and-variant-calling-methods</link>
	<title><![CDATA[VG: variation graph data structures, interchange formats, alignment, genotyping, and variant calling methods]]></title>
	<description><![CDATA[<p><em>Variation graphs</em>&nbsp;provide a succinct encoding of the sequences of many genomes. A variation graph (in particular as implemented in vg) is composed of:</p>
<ul>
<li><em>nodes</em>, which are labeled by sequences and ids</li>
<li><em>edges</em>, which connect two nodes via either of their respective ends</li>
<li><em>paths</em>, describe genomes, sequence alignments, and annotations (such as gene models and transcripts) as walks through nodes connected by edges</li>
</ul><p>Address of the bookmark: <a href="https://github.com/vgteam/vg" rel="nofollow">https://github.com/vgteam/vg</a></p>]]></description>
	<dc:creator>Jit</dc:creator>
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