Mercurial > repos > jjohnson > trinityrnaseq
view transcriptsToOrfs.xml @ 9:09c1e388c20c default tip
Change samtools tool_dependency to iuc package_samtools_0_1_19
author | Jim Johnson <jj@umn.edu> |
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date | Thu, 06 Feb 2014 10:45:40 -0600 |
parents | 5eb99d21ef0d |
children |
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<tool id="transcriptsToOrfs" name="transcriptsToOrfs" version="0.0.2"> <description>Trinity Transcripts to Candidate Peptides</description> <requirements> <requirement type="package" version="2013_08_14">trinityrnaseq</requirement> <requirement type="package" version="3.0">hmmer</requirement> </requirements> <command> \$TRINITY_HOME/trinity-plugins/transdecoder/transcripts_to_best_scoring_ORFs.pl -t $transcripts #if $min_prot_length: -m $min_prot_length #end if #if $retain_long_orfs: --retain_long_orfs $retain_long_orfs #end if #if $training_count: -T $training_count #end if #if str($strand_specificity) == 'SS': -S #end if #if $genetic_code.__str__ != '': -G $genetic_code #end if #if $search.use_pfam == 'yes': --search_pfam "${ filter( lambda x: str( x[0] ) == str( $search.pfam_db ), $__app__.tool_data_tables[ 'pfam_databases' ].get_fields() )[0][-1] }" --CPU $search.CPU #end if </command> <inputs> <param format="fasta" name="transcripts" type="data" label="Transcripts sequences in fastA format" help="" /> <param name="min_prot_length" type="integer" value="" optional="true" label="Minimum peptide length (in amino acids)" help="default: 100"> <validator type="in_range" message="Minimum peptide length should be at least 50" min="50" /> </param> <param name="retain_long_orfs" type="integer" value="" optional="true" label="Retain all ORFs found that are of minimum length in nucleotides" help="default: 900" > <validator type="in_range" message="ORF length should be at least 50" min="50" /> </param> <param name="training_count" type="integer" value="" optional="true" label="Number of top longest ORFs to train Markov Model (hexamer stats)" help="default: 500" > <validator type="in_range" message="ORF count should be at least 50" min="50" /> </param> <param name="strand_specificity" type="select" label="Strand specificity type"> <option value="DS">NOT strand specific, examine both strands</option> <option value="SS">Strand specific, examine only top strand</option> </param> <param name="genetic_code" type="select" label="Genetic Code"> <option value="">use default(universal)</option> <option value="universal">universal</option> <option value="Euplotes">Euplotes</option> <option value="Tetrahymena">Tetrahymena</option> <option value="Candida">Candida</option> <option value="Acetabularia">Acetabularia</option> </param> <conditional name="search"> <param name="use_pfam" type="select" label="Search PFAM database"> <option value="no">NO</option> <option value="yes">YES</option> </param> <when value="no"/> <when value="yes"> <param name="pfam_db" type="select" label="Pfam database"> <options from_data_table="pfam_databases" /> </param> <param name="CPU" type="integer" value="2" min="1" label="CPU" help="Number of CPUs to use by hmmscan" /> </when> </conditional> </inputs> <stdio> <exit_code range="1:" level="fatal" description="Failed" /> <regex match="Error" source="stderr" level="fatal" description="Failed" /> </stdio> <outputs> <data format="txt" name="trinity_pep_pfam" label="${tool.name} on ${on_string}: Pfam matches to Candidate Peptide Sequences" from_work_dir="longest_orfs.pep.pfam.dat"> <filter>search['use_pfam'] == 'yes'</filter> </data> <data format="gff3" name="trinity_pep_gff3" label="${tool.name} on ${on_string} Candidate Peptide Features" from_work_dir="best_candidates.eclipsed_orfs_removed.gff3" /> <data format="bed" name="trinity_pep_bed" label="${tool.name} on ${on_string} Candidate Peptide Coordinates" from_work_dir="best_candidates.eclipsed_orfs_removed.bed" /> <data format="fasta" name="trinity_pep_cds" label="${tool.name} on ${on_string}: Candidate Peptide CDS Sequences" from_work_dir="best_candidates.eclipsed_orfs_removed.cds"/> <data format="fasta" name="trinity_pep_seqs" label="${tool.name} on ${on_string}: Candidate Peptide Sequences" from_work_dir="best_candidates.eclipsed_orfs_removed.pep"/> </outputs> <tests> <test> <param name="transcripts" ftype="fasta" value="TrinitySingle.fasta"/> <param name="min_prot_length" value="100"/> <param name="use_pfam" value="no"/> <output name="trinity_pep_seqs"> <assert_contents> <has_text text="WAAKAWLITARSLYPADF" /> </assert_contents> </output> <output name="trinity_pep_cds"> <assert_contents> <has_text text="TGGGCAGCCAAGGCATGGCTGATCACGGCCCGCA" /> </assert_contents> </output> <output name="trinity_pep_bed"> <assert_contents> <has_text text="comp10_c0_seq1" /> </assert_contents> </output> <output name="trinity_pep_gff3"> <assert_contents> <has_text text="comp10_c0_seq1" /> </assert_contents> </output> </test> </tests> <help> ** transcriptsToOrfs ** Trinity_ is a de novo transcript assembler that uses RNA-seq data as input. This tool searches for open reading frames in the assembled transcripts. .. _Trinity: http://trinityrnaseq.sourceforge.net </help> </tool>