Trinity r20131110: Difference between revisions
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/cm/shared/modulefiles/SHARED/ | /cm/shared/modulefiles/SHARED/ | ||
< | <pre> | ||
#%Module1.0####################################################################### | #%Module1.0####################################################################### | ||
## Trinity r20131110 modulefile | ## Trinity r20131110 modulefile | ||
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module-whatis "Adds Trinity r20131110 to your environment" | module-whatis "Adds Trinity r20131110 to your environment" | ||
module load bowtie/1-1.0.0 | |||
set trinity_r20131110_root /cm/shared/apps/SHARED/Trinity/trinityrnaseq_r20131110/ | set trinity_r20131110_root /cm/shared/apps/SHARED/Trinity/trinityrnaseq_r20131110/ | ||
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prepend-path PATH $trinity_r20131110_root | prepend-path PATH $trinity_r20131110_root | ||
</pre> | |||
</ | |||
== Installation details == | == Installation details == | ||
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http://sourceforge.net/projects/trinityrnaseq/files/ | http://sourceforge.net/projects/trinityrnaseq/files/ | ||
Building of Inchworm and Chrysalis was done by simply issuing: | Building of Inchworm and Chrysalis was done by simply issuing: | ||
< | <pre> | ||
make | make | ||
</ | </pre> | ||
Latest revision as of 15:45, 15 June 2023
Trinity, developed at the Broad Institute and the Hebrew University of Jerusalem, 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:
- Inchworm 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.
- Chrysalis 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.
- Butterfly 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.
Module file
The module file can be found in this location:
/cm/shared/modulefiles/SHARED/
#%Module1.0####################################################################### ## Trinity r20131110 modulefile ## proc ModulesHelp { } { puts stderr "\tAdds Trinity r20131110 to your environment" } module-whatis "Adds Trinity r20131110 to your environment" module load bowtie/1-1.0.0 set trinity_r20131110_root /cm/shared/apps/SHARED/Trinity/trinityrnaseq_r20131110/ prepend-path PATH $trinity_r20131110_root
Installation details
The source was downloaded from SourceForge on 15-03-2014:
http://sourceforge.net/projects/trinityrnaseq/files/
Building of Inchworm and Chrysalis was done by simply issuing:
make