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view pyCRAC/pyMotif.xml @ 1:7c9574213c0a draft default tip
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author | swebb |
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date | Thu, 20 Jun 2013 12:13:43 -0400 |
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<tool id ="pyMotif" name="pyMotif"> <requirements> <requirement type="package">pyCRAC</requirement> </requirements> <command interpreter="perl"> pyMotif.pl -f $input --gtf=$addGTF.gtf #if $addGTF.gtfFile == "default" and $addGTF.annotate.annotations == "auto": --annotation $addGTF.annotate.scan.annotation #else: --annotation $addGTF.annotate.annotation #end if# --tab=$addTab.tab #if $addOpt.options == "edit": --options --k_min $addOpt.kmin --k_max $addOpt.kmax --numberofkmers=$addOpt.numberofkmers --overlap $addOpt.overlap --range $addOpt.range #end if# -o "$input.name" --id $count.id --count $count --random $random --features $features --zscores $zscores </command> <version_command>/usr/local/bin/pyMotif.py --version</version_command> <inputs> <param format="gtf" name="input" type="data" label="Input File --input_file" help="File of type .gtf" /> <conditional name="addTab"> <param name="tabFile" type="select" label="Choose Genomic Reference Sequence from"> <option value="default" selected="true">Defaults</option> <option value="other">History</option> </param> <when value="default"> <param name="tab" type="select" label="Genomic Reference Sequence --tab" help="Tab file containing genomic reference sequence"> <options from_data_table="pycrac_tab"/> </param> </when> <when value="other"> <param format="tabular" name="tab" type="data" label="Genomic Reference Sequence --tab" help="Tab file containing genomic reference sequence"/> </when> </conditional> <conditional name="addGTF"> <param name="gtfFile" type="select" label="Choose GTF File from"> <option value="default" selected="true">Defaults</option> <option value="other">History</option> </param> <when value="default"> <param name="gtf" type="select" label="GTF File --gtf" help="GTF file containing gene ID co-ordinates"> <options from_data_table="pycrac_gtf"/> </param> <conditional name="annotate"> <param name="annotations" type="select" label="Select annotation"> <option value="all" selected="true">All</option> <option value="manual">Enter in text box</option> <option value="auto">Scan pyGetGTFSources file</option> </param> <when value="all"> <param name="annotation" type="hidden" format="txt" size="10" value="all"/> </when> <when value="manual"> <param name="annotation" type="text" format="txt" size="100" value="protein_coding" label="Select which annotation to focus search on --annotation" help="To find a list of available annotations please use pyGetGTFSources tool"> <validator type="empty_field" message="Please enter a value"/> </param> </when> <when value="auto"> <param format="tabular" name="gtf_annotation" type="data" label="GTF annotation File (pyGetGTFSources output)" help="Tabular file containing unique list of annotations/sources in selected GTF file. Refer to pyGetGTFSources"/> <conditional name="scan"> <param name="annotations" type="select" label="Scan this file for annotations" help="Choose the correct GTF file then choose GO"> <option value="wait" selected="true">Waiting</option> <option value="scanning">Go</option> </param> <when value="wait"> </when> <when value="scanning"> <param name="annotation" type="select" multiple="false" label="Select which annotation to focus search on --annotation"> <options from_dataset="gtf_annotation"> <column name="name" index="0"/> <column name="value" index="0"/> </options> </param> </when> </conditional> </when> </conditional> </when> <when value="other"> <param format="gtf" name="gtf" type="data" label="GTF File --gtf" help="GTF file containing gene ID co-ordinates"/> <conditional name="annotate"> <param name="annotations" type="select" label="Select annotation"> <option value="all" selected="true">All</option> <option value="manual">Enter in text box</option> <option value="auto">Scan selected file</option> </param> <when value="all"> <param name="annotation" type="hidden" format="txt" size="10" value="all"/> </when> <when value="manual"> <param name="annotation" type="text" format="txt" size="100" value="protein_coding" label="Select which annotation to focus search on --annotation" help="To find a list of available annotations please use pyGetGTFSources tool"> <validator type="empty_field" message="Please enter a value"/> </param> </when> <when value="auto"> <param name="annotation" type="select" multiple="false" label="Select which annotation to focus search on --annotation"> <options from_dataset="gtf"> <column name="name" index="1"/> <column name="value" index="1"/> <filter type="unique_value" name="unique" column="1"/> </options> </param> </when> </conditional> </when> </conditional> <conditional name="addOpt"> <param name="options" type="select" label="Standard options"> <option value="default" selected="true">Default</option> <option value="edit">Edit</option> </param> <when value="edit"> <param format="integer" name="kmin" type="integer" label="Minimum k-mer Length --k_min " value="4" size="6" help="Set the minimal k-mer length"> <validator type="in_range" min="1" message="Please enter a value >= 1"/> </param> <param format="integer" name="kmax" type="integer" label="Maximum k-mer Length --k_min " value="8" size="6" help="Set the minimal k-mer length"> <validator type="in_range" min="0" message="Please enter a value >= 0"/> </param> <param format="integer" name="numberofkmers" type="integer" label="Maximum number of k-mers in output file --numberofkmers" value="1000" size="6" help="Set the maximum number of k-mers in output"> <validator type="in_range" min="0" message="Please enter a value >= 0"/> </param> <param format="integer" name="range" type="integer" label="Range --range" value="0" size="5" help="Manually set the length of the 5' and 3' UTRs 0>50000"> <validator type="in_range" min="0" max="50000" message="Please enter a value between 0 and 50000"/> </param> <param format="integer" name="overlap" type="integer" label="Overlap --overlap" value="1" size="5" help="Sets the number of nucleotides a read has to overlap with a gene before it is considered a hit. "> <validator type="in_range" min="1" message="Please enter a positive integer"/> </param> </when> <when value="default"> </when> </conditional> <param name="label" type="text" format="txt" size="30" value="pyMotif" label="Enter output file label -o" /> </inputs> <outputs> <data format="tabular" name="zscores" label="${label.value}_k-mer_Z_scores.txt"/> <data format="tabular" name="count" label="${label.value}_data_k-mers_count.txt"/> <data format="gtf" name="features" label="${label.value}_top_k-mers_in_features.gtf"/> <data format="tabular" name="random" label="${label.value}_random_k-mers_count.txt"/> </outputs> <help> .. class:: infomark **pyMotif** pyMotif is part of the pyCRAC_ package. Looks for enriched sequence motifs in high-throughput sequencing data. Produces a GTF type output file with coordinates and Z-scores for enriched motifs. The GTF file can be visualised in genome browsers. .. _pyCRAC: http://sandergranneman.bio.ed.ac.uk/Granneman_Lab/pyCRAC_software.html ------ **Parameter list** File input options:: -f intervals.gtf, --input_file=intervals.gtf Provide the path to an interval gtf file. By default it expects data from the standard input. -o OUTPUT_FILE, --output_file=OUTPUT_FILE Use this flag to override the standard file names. Do NOT add an extension. --gtf=annotation_file.gtf type the path to the gtf annotation file that you want to use --tab=tab_file.tab type the path to the tab file that contains the genomic reference sequence pyMotif specific options:: --k_min=4 this option allows you to set the shortest k-mer length. Default = 4. --k_max=6 this option allows you to set the longest k-mer length. Default = 8. -n 100, --numberofkmers=100 choose the maximum number of enriched k-mer sequences you want to have reported in output files. Default = 1000 pyCRAC common options:: -a protein_coding, --annotation=protein_coding select which annotation (i.e. protein_coding, ncRNA, sRNA, rRNA,snoRNA,snRNA, depending on the source of your GTF file) you would like to focus your search on. Default = all annotations -r 100, --range=100 allows you to add regions flanking the genomic feature. If you set '-r 50' or '--range=50', then the program will add 50 nucleotides to each feature on each side regardless of whether the GTF file has genes with annotated UTRs. --overlap=1 sets the number of nucleotides a motif has to overlap with a genomic feature before it is considered a hit. Default = 1 nucleotide </help> </tool>