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	<title><![CDATA[BOL: RNA-Seq De novo Assembly Using Trinity]]></title>
	<link>https://bioinformaticsonline.com/bookmarks/view/26752/rna-seq-de-novo-assembly-using-trinity?</link>
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	<guid isPermaLink="true">https://bioinformaticsonline.com/bookmarks/view/26752/rna-seq-de-novo-assembly-using-trinity</guid>
	<pubDate>Wed, 23 Mar 2016 05:53:46 -0500</pubDate>
	<link>https://bioinformaticsonline.com/bookmarks/view/26752/rna-seq-de-novo-assembly-using-trinity</link>
	<title><![CDATA[RNA-Seq De novo Assembly Using Trinity]]></title>
	<description><![CDATA[<p>Trinity, developed at the <a href="http://www.broadinstitute.org">Broad Institute</a> and the <a href="http://www.cs.huji.ac.il">Hebrew University of Jerusalem</a>, represents a novel method for the efficient and robust de novo reconstruction of transcriptomes from RNA-seq data. Trinity combines three independent software modules: Inchworm, Chrysalis, and Butterfly, applied sequentially to process large volumes of RNA-seq reads. Trinity partitions the sequence data into many individual de Bruijn graphs, each representing the transcriptional complexity at at a given gene or locus, and then processes each graph independently to extract full-length splicing isoforms and to tease apart transcripts derived from paralogous genes. Briefly, the process works like so:</p>
<ul>
<li>
<p><em>Inchworm</em> assembles the RNA-seq data into the unique sequences of transcripts, often generating full-length transcripts for a dominant isoform, but then reports just the unique portions of alternatively spliced transcripts.</p>
</li>
<li>
<p><em>Chrysalis</em> clusters the Inchworm contigs into clusters and constructs complete de Bruijn graphs for each cluster. Each cluster represents the full transcriptonal complexity for a given gene (or sets of genes that share sequences in common). Chrysalis then partitions the full read set among these disjoint graphs.</p>
</li>
<li>
<p><em>Butterfly</em> then processes the individual graphs in parallel, tracing the paths that reads and pairs of reads take within the graph, ultimately reporting full-length transcripts for alternatively spliced isoforms, and teasing apart transcripts that corresponds to paralogous genes.</p>
</li>
</ul>
<p>More at https://github.com/trinityrnaseq/trinityrnaseq/wiki</p>
<p>......................................................................................................................................</p>
<p>Download Trinity <a href="https://github.com/trinityrnaseq/trinityrnaseq/releases">here</a>.</p>
<p>Build Trinity by typing 'make' in the base installation directory.</p>
<p>Assemble RNA-Seq data like so:</p>
<pre><code> Trinity --seqType fq --left reads_1.fq --right reads_2.fq --CPU 6 --max_memory 20G 
</code></pre>
<p>Find assembled transcripts as: 'trinity_out_dir/Trinity.fasta'</p><p>Address of the bookmark: <a href="https://github.com/trinityrnaseq/trinityrnaseq/wiki" rel="nofollow">https://github.com/trinityrnaseq/trinityrnaseq/wiki</a></p>]]></description>
	<dc:creator>Surabhi Chaudhary</dc:creator>
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