Mercurial > repos > iuc > meme_fimo
diff fimo.xml @ 5:eca84de658b0 draft
Uploaded
author | iuc |
---|---|
date | Fri, 17 Jun 2016 13:15:48 -0400 |
parents | 0fce5521bb96 |
children | cdcc4bb60bc3 |
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--- a/fimo.xml Tue Mar 08 08:10:52 2016 -0500 +++ b/fimo.xml Fri Jun 17 13:15:48 2016 -0400 @@ -1,4 +1,4 @@ -<tool id="meme_fimo" name="FIMO" version="4.11.0.2"> +<tool id="meme_fimo" name="FIMO" version="4.11.0.3"> <description>- Scan a set of sequences for motifs.</description> <requirements> <requirement type="package" version="6.9.3">imagemagick</requirement> @@ -6,6 +6,7 @@ </requirements> <command> <![CDATA[ + mkdir -p output && python $__tool_directory__/fimo_wrapper.py --input_motifs "${input_motifs}" #if str($fasta_type.fasta_type_selector) == 'history': @@ -28,10 +29,14 @@ --motif "${motif.motif}" #end for #end if + --output_separate_motifs ${options_type.output_separate_motifs} --motif_pseudo "${options_type.motif_pseudo}" ${options_type.no_qvalue} ${options_type.norc} - ${options_type.parse_genomic_coord} + #if str($options_type.parse_genomic_coord_cond.parse_genomic_coord) == 'yes': + --parse_genomic_coord 'yes' + --remove_duplicate_coords ${options_type.parse_genomic_coord_cond.remove_duplicate_coords} + #end if #if str($options_type.psp_cond.psp_selector) == 'yes': --input_psp "${input_psp}" #end if @@ -99,10 +104,23 @@ </repeat> </when> </conditional> + <param name="output_separate_motifs" type="select" label="Output a dataset per motif?" help="Output a collection consisting of a separate dataset for each motif in the input"> + <option value="no" selected="true">No</option> + <option value="yes">Yes</option> + </param> <param name="motif_pseudo" type="float" value="0.1" label="Pseudocount to add to counts in motif matrix" help="A pseudocount to be added to each count in the motif matrix, after first multiplying by the corresponding background frequency"/> <param name="no_qvalue" label="Do not compute a q-value for each p-value" type="boolean" truevalue="--no_qvalue" falsevalue="" checked="True" help="The q-value calculation is that of Benjamini and Hochberg (1995)."/> <param name="norc" label="Do not score the reverse complement DNA strand" type="boolean" truevalue="--norc" falsevalue="" checked="False" /> - <param name="parse_genomic_coord" label="Check each sequence header for UCSC style genomic coordinates" type="boolean" truevalue="--parse_genomic_coord" falsevalue="" checked="False" /> + <conditional name="parse_genomic_coord_cond"> + <param name="parse_genomic_coord" label="Check each sequence header for UCSC style genomic coordinates" type="select"> + <option value="no" selected="true">No</option> + <option value="yes">Yes</option> + </param> + <when value="yes"> + <param name="remove_duplicate_coords" type="boolean" truevalue="yes" falsevalue="no" label="Remove duplicate entries in unique GFF coordinates?" help="Remove duplicate entries as defined by the unique GFF coordinates" /> + </when> + <when value="no"/> + </conditional> <conditional name="psp_cond"> <param name="psp_selector" type="select" label="Use position-specific priors?"> <option value="no" selected="true">No</option> @@ -160,6 +178,7 @@ </actions> </data> <data format="tabular" name="gff_outfile" label="${tool.name} on ${on_string} (almost-gff)"> + <filter>options_type['output_separate_motifs'] == 'no'</filter> <actions> <conditional name="fasta_type.fasta_type_selector"> <when value="cached"> @@ -172,6 +191,10 @@ </conditional> </actions> </data> + <collection name="motifs" type="list" label="Motifs: ${tool.name} on ${on_string}"> + <discover_datasets pattern="(?P<designation>.*)" directory="output" ext="gff" visible="false" /> + <filter>options_type['output_separate_motifs'] == 'yes'</filter> + </collection> <data format="cisml" name="xml_outfile" label="${tool.name} on ${on_string} (xml)"> <actions> <conditional name="fasta_type.fasta_type_selector"> @@ -209,7 +232,7 @@ <output name="html_outfile" file="fimo_output_html_1.html" compare="contains"/> <output name="txt_outfile" file="fimo_output_txt_1.txt" compare="contains"/> <output name="gff_outfile" file="fimo_output_almost-gff_1.txt" compare="contains"/> - <output name="xml_outfile" file="fimo_output_xml_1.xml" lines_diff="8"/> + <output name="xml_outfile" file="fimo_output_xml_1.xml" compare="contains"/> <output name="interval_outfile" file="fimo_output_interval_1.txt" compare="contains"/> </test> <test> @@ -221,7 +244,24 @@ <output name="html_outfile" file="fimo_output_html_2.html" compare="contains"/> <output name="txt_outfile" file="fimo_output_txt_2.txt" compare="contains"/> <output name="gff_outfile" file="fimo_output_almost-gff_2.txt" compare="contains"/> - <output name="xml_outfile" file="fimo_output_xml_2.xml" lines_diff="8"/> + <output name="xml_outfile" file="fimo_output_xml_2.xml" compare="contains"/> + <output name="interval_outfile" file="fimo_output_interval_2.txt" compare="contains"/> + </test> + <test> + <param name="input_motifs" value="meme_output_xml_1.xml" ftype="memexml"/> + <param name="fasta_type_selector" value="history"/> + <param name="input_database" value="phiX.fasta" ftype="fasta"/> + <param name="options_type_selector" value="advanced"/> + <param name="parse_genomic_coord" value="--parse_genomic_coord"/> + <param name="remove_duplicate_coords" value="yes"/> + <param name="output_separate_motifs" value="yes"/> + <param name="non_commercial_use" value="True"/> + <output name="html_outfile" file="fimo_output_html_2.html" compare="contains"/> + <output name="txt_outfile" file="fimo_output_txt_2.txt" compare="contains"/> + <output_collection name="motifs" type="list"> + <element name="MOTIF1.gff" file="motif1.gff" ftype="gff" compare="contains"/> + </output_collection> + <output name="xml_outfile" file="fimo_output_xml_2.xml" compare="contains"/> <output name="interval_outfile" file="fimo_output_interval_2.txt" compare="contains"/> </test> </tests> @@ -235,7 +275,7 @@ FIMO scans a sequence database for individual matches to each of the motifs you provide (sample output for motifs and sequences). The name FIMO stands for 'Find Individual Motif Occurrences'. The program searches a database of sequences for occurrences of known motifs, treating each motif independently. Motifs must be in MEME Motif Format. You can define the statistical threshold -(p-value) for motifs and whether FIMO scans just the given sequences or their reverse complements (where applicable), too. +(p-value) for motifs and whether FIMO scans just the given sequences or their reverse complements (where applicable). .. class:: infomark