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author | trinity_ctat |
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date | Tue, 17 Jul 2018 11:50:42 -0400 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/ctat_trinity_rnaseq.xml Tue Jul 17 11:50:42 2018 -0400 @@ -0,0 +1,154 @@ +<tool id="ctat_trinity_rnaseq" name="ctat_trinity_rnaseq" version="1.0.0" profile="17.05"> + + <!-- Original tool written by Jeremy Goecks, + later development/maintenance by (in chronological order) + Brian Haas, Ben Fulton, Cicada Dennis + --> + <description>De novo assembly of RNA-Seq data using Trinity</description> + <requirements> + <requirement type="package" version="2.7">python</requirement> + <requirement type="package">subprocess32</requirement> + <requirement type="package">bzip2</requirement> + <requirement type="package" version="1.3.0">rsem</requirement> + <requirement type="package" version="3">bioconductor-edger</requirement> + <requirement type="package" version="2">bioconductor-qvalue</requirement> + <requirement type="package" version="2.6.6">trinity</requirement> + </requirements> + <command detect_errors="default"> + <![CDATA[ + python $__tool_directory__/ctat_trinity_wrapper.py + --CPU \${GALAXY_SLOTS:-4} + --max_memory \${TRINITY_MAX_MEMORY:-31G} + #if str($inputs.paired_or_single) == "paired": + --left $inputs.left_input --right $inputs.right_input + #if $inputs.left_input.ext == 'fasta': + --seqType fa + #else: + --seqType fq + #end if + #else: + --single $inputs.input + #if $inputs.input.ext == 'fasta': + --seqType fa + #else: + --seqType fq + #end if + #end if + ## direct to output + --timing trinity_out_dir/Trinity.timing + --log $trinity_log + + ]]> + <!-- The fullpath, dir, and user options (preceed with dashes) can be + used in the ctat_trinity_wrapper.py command to create rerunable jobs. + We are not supporting rerunable jobs in this release of this tool. + fullpath \${TRINITY_RERUN_PREFIX} + dir '$adv.rerundir' + user $__user_id__ + mem_per_cpu 31 + --> + </command> + <stdio> + <exit_code range="1:" level="fatal" description="Program failed" /> + <exit_code range=":-1" level="fatal" description="DRM killed job" /> + </stdio> + <inputs> + <conditional name="inputs"> + <param name="paired_or_single" type="select" label="Paired or Single-end data?"> + <option value="paired">Paired</option> + <option value="single">Single</option> + </param> + <when value="paired"> + <param format="fasta,fastq" name="left_input" type="data" label="Left/Forward strand reads" help=""/> + <param format="fasta,fastq" name="right_input" type="data" label="Right/Reverse strand reads" help=""/> + </when> + <when value="single"> + <param format="fasta,fastq" name="input" type="data" label="Single-end reads" help=""/> + </when> + </conditional> + <!-- The following section was used to aid in creating rerunable jobs. + We are not supporting rerunable jobs in this release of this tool. + <section name="adv" title="Allow Job Rerun" expanded="False"> + <param name="rerundir" type="txt" size="10" label="To make a job rerunnable, you will need to specify a unique tag to label the job, with no spaces or wierd characters." /> + </section> + --> + </inputs> + <outputs> + <data format="txt" name="trinity_log" label="${tool.name} on ${on_string}: log" /> + <data format="fasta" name="assembled_transcripts" label="${tool.name} on ${on_string}: Assembled Transcripts" from_work_dir="trinity_out_dir/Trinity.fasta"/> + </outputs> + <tests> + <!-- Not testing with the following inputs anymore. + <param name="left_input" value="FLI1.left.fq" /> + <param name="right_input" value="FLI1.right.fq" /> + --> + <test> + <param name="paired_or_single" value="paired" /> + <param name="left_input" value="reads.left.simPE.fq" /> + <param name="right_input" value="reads.right.simPE.fq" /> + <!-- Not using in public version of tool + <param name="adv.rerundir" value="planemo_test_1" /> + --> + <output name="trinity_log" > + <assert_contents> + <has_line_matching expression=".+" /> + <has_line line="Trinity exited with status 0" /> + </assert_contents> + </output> + <output name="assembled_transcripts" > + <assert_contents> + <has_line_matching expression=".+" /> + <has_line_matching expression=">TRINITY.+?len=.+?path=.+" /> + </assert_contents> + </output> + </test> + <test> + <param name="paired_or_single" value="paired" /> + <param name="left_input" value="Sp.cat_ds_hs.left.fq" /> + <param name="right_input" value="Sp.cat_ds_hs.right.fq" /> + <!-- Not using in public version of tool + <param name="adv.rerundir" value="planemo_test_2" /> + --> + <!-- Following parameters are not used in this version of this tool. --> + <!-- + <param name="JM" value="50G" /> + <param name="CPU" value="2" /> + <param name="library_type" value="None" /> + <param name="group_pairs_distance" value="500" /> + <param name="path_reinforcement_distance" value="75" /> + <param name="use_additional" value="no" /> + --> + <output name="trinity_log" > + <assert_contents> + <has_line_matching expression=".+" /> + <has_line line="Trinity exited with status 0" /> + </assert_contents> + </output> + <output name="assembled_transcripts" > + <assert_contents> + <has_line_matching expression=".+" /> + <has_line_matching expression=">TRINITY.+?len=.+?path=.+" /> + </assert_contents> + </output> + </test> + </tests> + <help> +This instance runs Trinity with the following command: + + Trinity --max_memory 31G --CPU 4 --seqType seq_type --single singlefile or --left left_file --right right_file + +Define TRINITY_MAX_MEMORY and GALAXY_SLOTS to change the default values for --max_memory and --CPU, respectively. + +.. class:: infomark + +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 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. For more information, visit Trinity's wiki page here_. + +.. _Trinity: https://github.com/trinityrnaseq/trinityrnaseq/wiki +.. _here: https://github.com/trinityrnaseq/trinityrnaseq/wiki + </help> + + <citations> + <citation type="doi">10.1038/nbt.1883</citation> + </citations> + +</tool>