# HG changeset patch # User nate # Date 1474639315 14400 # Node ID 976e99dd3c2be11b85593a95fae039920a4585f1 # Parent d0c258caafaf7adf0e45ceb214e0b0d620b44c54 New version for Bridges diff -r d0c258caafaf -r 976e99dd3c2b trinityrnaseq.xml --- a/trinityrnaseq.xml Tue Sep 01 16:15:38 2015 -0400 +++ b/trinityrnaseq.xml Fri Sep 23 10:01:55 2016 -0400 @@ -2,19 +2,28 @@ - (Beta) De novo assembly of RNA-Seq data Using Trinity on PSC's Greenfield + (Beta) De novo assembly of RNA-Seq data Using Trinity on PSC's Bridges - - bowtie - samtools + + bowtie + samtools java - trinity + perl + trinity - MEM=`expr "\${GALAXY_SLOTS:-15}" \* 50 - 16` ; + MEM=`expr "\${GALAXY_SLOTS:-16}" \* 48 - 16` ; + + workdir=`pwd`; + echo "workdir is \$workdir"; + cd \$LOCAL; + echo "Running Trinity from `pwd`"; + Trinity --max_memory "\${MEM}G" --CPU "\${GALAXY_SLOTS:-16}" - --bflyHeapSpaceMax "\${MEM}G" + --bflyHeapSpaceMax "32G" + --bflyHeapSpaceInit "2G" + --bflyGCThreads "6" ## Inputs. #if str($inputs.paired_or_single) == "paired": @@ -52,7 +61,10 @@ > $trinity_log 2>&1 ## if Trinity fails, output the end of the log to stderr for Galaxy, and touch the output file for Pulsar - || (ec=\$? ; cat $trinity_log >&2 ; mkdir -p trinity_out_dir ; touch trinity_out_dir/Trinity.fasta ; exit \$ec) + || (ec=\$? ; cp -pr . \$workdir; cd \$workdir; cat $trinity_log >&2 ; mkdir -p trinity_out_dir ; touch trinity_out_dir/Trinity.fasta ; exit \$ec); + + cp -pr . \$workdir; + cd \$workdir; @@ -109,12 +121,12 @@ -.. warning:: This version of Trinity, which runs on Greenfield_ at the `Pittsburgh Supercomputing Center`_, is a **beta** version. It may not be possible to rerun the same version of this tool, Trinity itself, or its other dependencies (Bowtie, SAMtools) in the future. **When rerunning this tool on the same data, it should, but cannot be guaranteed to reproduce the exact same results to the level of certainty as other Galaxy tools.** +.. warning:: This version of Trinity, which runs on Bridges_ at the `Pittsburgh Supercomputing Center`_, is a **beta** version. It may not be possible to rerun the same version of this tool, Trinity itself, or its other dependencies (Bowtie, SAMtools) in the future. **When rerunning this tool on the same data, it should, but cannot be guaranteed to reproduce the exact same results to the level of certainty as other Galaxy tools.** Trinity is a de novo transcript assembler that uses RNA-seq data as input. This tool runs all Trinity_ commands--Inchworm, Chrysalis, and Butterfly--in a single pass. .. _Trinity: http://trinityrnaseq.github.io .. _Pittsburgh Supercomputing Center: http://www.psc.edu -.. _Greenfield: http://www.psc.edu/index.php/resources-for-users/computing-resources/greenfield +.. _Bridges: http://www.psc.edu/bridges