Mercurial > repos > gkumar09 > trinityrnaseq_protocol
comparison transcriptsToOrfs.xml @ 14:e2e6533f2514 draft
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| author | gkumar09 |
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| date | Wed, 23 Sep 2015 15:24:38 -0400 |
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| 13:8bf618c08b4d | 14:e2e6533f2514 |
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| 1 <tool id="transcriptsToOrfs" name="transcriptsToOrfs" version="0.0.1"> | |
| 2 | |
| 3 <description>Trinity Transcripts to Candidate Peptides</description> | |
| 4 <requirements> | |
| 5 <requirement type="package">trinity</requirement> | |
| 6 </requirements> | |
| 7 <command interpreter="python"> | |
| 8 trinityToolWrapper.py Analysis/Coding/transcripts_to_best_scoring_ORFs.pl | |
| 9 | |
| 10 -t $transcripts | |
| 11 -m $min_prot_length | |
| 12 --CPU $CPU | |
| 13 --search_pfam "${ filter( lambda x: str( x[0] ) == str( $pfam_db ), $__app__.tool_data_tables[ 'pfam_databases' ].get_fields() )[0][-1] }" | |
| 14 | |
| 15 #if str($strand_specificity) == 'SS': | |
| 16 -S | |
| 17 #end if | |
| 18 | |
| 19 ## direct to output | |
| 20 > output | |
| 21 | |
| 22 </command> | |
| 23 <inputs> | |
| 24 | |
| 25 <param format="fasta" name="transcripts" type="data" label="Transcripts sequences in fastA format" help="" /> | |
| 26 | |
| 27 <param name="min_prot_length" type="integer" label="Minimum peptide length (in amino acids)" value="100" min="50" help="" /> | |
| 28 | |
| 29 <param name="strand_specificity" type="select" label="Strand specificity type"> | |
| 30 <option value="DS">NOT strand specific, examine both strands</option> | |
| 31 <option value="SS">Strand specific, examine only top strand</option> | |
| 32 </param> | |
| 33 | |
| 34 <param name="pfam_db" type="select" label="Pfam database"> | |
| 35 <options from_data_table="pfam_databases" /> | |
| 36 </param> | |
| 37 | |
| 38 <param name="CPU" type="integer" value="2" min="1" label="CPU" help="Number of CPUs to use by hmmscan" /> | |
| 39 | |
| 40 </inputs> | |
| 41 <outputs> | |
| 42 <data format="txt" name="trinity_pep_pfam" label="${tool.name} on ${on_string}: Pfam matches to Candidate Peptide Sequences" from_work_dir="longest_orfs.pep.pfam.dat"/> | |
| 43 <data format="fasta" name="trinity_pep_seqs" label="${tool.name} on ${on_string}: Candidate Peptide Sequences" from_work_dir="best_candidates.eclipsed_orfs_removed.pep"/> | |
| 44 <data format="bed" name="trinity_pep_coords" label = "${tool.name} on ${on_string} Candidate Peptide Coordinates" from_work_dir="best_candidates.eclipsed_orfs_removed.bed" /> | |
| 45 </outputs> | |
| 46 <tests> | |
| 47 </tests> | |
| 48 <help> | |
| 49 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. | |
| 50 | |
| 51 .. _Trinity: http://trinityrnaseq.sourceforge.net | |
| 52 </help> | |
| 53 </tool> |
