Mercurial > repos > galaxyp > translate_bed_sequences
diff translate_bed_sequences.xml @ 0:d723eb657f1d draft
planemo upload for repository https://github.com/galaxyproteomics/tools-galaxyp/tree/master/tools/translate_bed_sequences commit e04ed4b4960d6109a85c1cc68a2bf4931c8751ef-dirty
author | galaxyp |
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date | Mon, 25 Jan 2016 12:21:21 -0500 |
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children | 6bbce76c78c1 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/translate_bed_sequences.xml Mon Jan 25 12:21:21 2016 -0500 @@ -0,0 +1,128 @@ +<?xml version="1.0"?> +<tool id="translate_bed_sequences" name="Translate BED Sequences" version="0.1.0"> + <description>3 frame translation of BED augmented with a sequence column</description> + <requirements> + <requirement type="package" version="1.62">biopython</requirement> + <requirement type="python-module">Bio</requirement> + </requirements> + <command interpreter="python"> + translate_bed_sequences.py --input "$input" + #if $fa_db: + --fa_db='$fa_db' + #end if + #if $fa_sep: + --fa_sep='$fa_sep' + #end if + #if $id_prefix: + --id_prefix='$id_prefix' + #end if + #if $reference: + --reference $reference + #else: + --reference ${input.metadata.dbkey} + #end if + #if $refsource: + --refsource $refsource + #end if + #if $seqtype: + --seqtype $seqtype + #end if + #if $score_name: + --score_name $score_name + #end if + #if $filter.filterseqs == 'yes': + #if $filter.leading_bp: + --leading_bp $filter.leading_bp + #end if + #if $filter.trailing_bp: + --trailing_bp $filter.trailing_bp + #end if + #else: + --unfiltered + #end if + #if $trim.trimseqs == 'no': + --untrimmed + #if str($trim.max_stop_codons) != '': + --max_stop_codons $trim.max_stop_codons + #end if + #end if + #if str($min_length) != '': + --min_length $min_length + #end if + --bed $translated_bed + --output "$output" + </command> + <inputs> + <param name="input" type="data" format="bed" label="BED file with added sequence column" + help="Output from 'Extract Genomic DNA' run on tophat junctions.bed "/> + <param name="fa_db" type="text" value="" optional="true" label="fasta ID source, e.g. generic" + help="Any Compomics application such as PeptideShaker, requires a source"> + </param> + <param name="fa_sep" type="text" value="" optional="true" label="fasta ID line separator character" + help="Only used when a fasta ID source is given, defaults to the pipe character"> + </param> + <param name="id_prefix" type="text" value="" optional="true" label="ID prefix for generated IDs" + help="Can be used to distinguish samples"> + <validator type="regex" message="Allowed chars:a-z A-Z 0-9 _ - |">^[a-zA-Z0-9_-|]*$</validator> + </param> + <param name="refsource" type="text" value="Ensembl" optional="true" label="Genome reference source" + help=""/> + <param name="reference" type="text" value="" optional="true" label="Genome reference name" + help="By default, the database metadata will be used."/> + <param name="seqtype" type="text" value="" optional="true" label="The SEQTYPE:STATUS to include in the fasta ID lines" + help="For example: pep:splice"/> + <param name="score_name" type="text" value="" optional="true" label="Add the bed score field fasta ID line with this tag name" + help="For example: with the tag name 'depth' and bed score 12: depth:12"/> + <conditional name="filter"> + <param name="filterseqs" type="select" label="Filter out translations with stop codons before the splice site"> + <option value="yes" selected="true">Yes</option> + <option value="no">No</option> + </param> + <when value="yes"> + <param name="leading_bp" type="integer" value="" min="0" optional="true" label="Stop codon filtering start position base pairs" + help="Do not reject translation is stop_codons are within base pairs of the BED start position for positive strand"/> + <param name="trailing_bp" type="integer" value="" min="0" optional="true" label="Stop codon filtering end position base pairs" + help="Do not reject translation is stop_codons are within base pairs of the BED end position for negative strand"/> + </when> + <when value="no"/> + </conditional> + <conditional name="trim"> + <param name="trimseqs" type="select" label="Trim translations to stop codons"> + <option value="yes" selected="true">Yes</option> + <option value="no">No</option> + </param> + <when value="no"> + <param name="max_stop_codons" type="integer" value="" min="0" optional="true" label="Maximum number of stop codons allowed in a translation to be reported"/> + </when> + </conditional> + <param name="min_length" type="integer" value="" min="0" optional="true" label="Minimum length of a translation to be reported"/> + </inputs> + <stdio> + <exit_code range="1:" level="fatal" description="Error" /> + </stdio> + <outputs> + <data name="translated_bed" metadata_source="input" format="bed" label="${tool.name} on ${on_string} bed"> + </data> + <data name="output" metadata_source="input" format="fasta" label="${tool.name} on ${on_string} fasta"> + </data> + </outputs> + <tests> + <test> + <param name="input" value="Extract_Genomic_DNA.bed" ftype="bed" dbkey="hg19"/> + <param name="reference" value="GRCh37"/> + <param name="seqtype" value="pep:novel"/> + <param name="score_name" value="depth"/> + <output name="output" file="translated_bed_sequences.fa"/> + </test> + </tests> + <help> +**Translate BED Sequences** + +This tool takes a BED input file that has been processed +by the Galaxy tool "Extract Genomic DNA" to add a 13th column with the transcript sequence. + +It generates a peptide fasta file with the 3-frame translations of the spliced sequence +defined by each entry in the input BED file. + + </help> +</tool>