Mercurial > repos > devteam > picard
view picard_CollectGcBiasMetrics.xml @ 4:2589e6207cb4 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tools/picard commit 33927a87ba2eee9bf0ecdd376a66241b17b3d734
author | devteam |
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date | Tue, 13 Oct 2015 12:27:49 -0400 |
parents | 52fdfc45590a |
children | 08f69add4d06 |
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<tool name="CollectGcBiasMetrics" id="picard_CollectGcBiasMetrics" version="@TOOL_VERSION@.0"> <description>charts the GC bias metrics</description> <macros> <import>picard_macros.xml</import> </macros> <expand macro="requirements"> <requirement type="package" version="3.1.2">R</requirement> </expand> <command> @java_options@ ##set up input files #set $reference_fasta_filename = "localref.fa" #if str( $reference_source.reference_source_selector ) == "history": ln -s "${reference_source.ref_file}" "${reference_fasta_filename}" && #else: #set $reference_fasta_filename = str( $reference_source.ref_file.fields.path ) #end if java -jar \$JAVA_JAR_PATH/picard.jar CollectGcBiasMetrics INPUT="${inputFile}" OUTPUT="${outFile}" CHART_OUTPUT="${pdfFile}" SUMMARY_OUTPUT="${summaryFile}" WINDOW_SIZE="${window_size}" MINIMUM_GENOME_FRACTION="${minimum_genome_fraction}" IS_BISULFITE_SEQUENCED="${is_bisulfite_sequenced}" REFERENCE_SEQUENCE="${reference_fasta_filename}" ASSUME_SORTED="${assume_sorted}" VALIDATION_STRINGENCY="${validation_stringency}" QUIET=true VERBOSITY=ERROR </command> <inputs> <param format="sam,bam" name="inputFile" type="data" label="Select SAM/BAM dataset or dataset collection" help="If empty, upload or import a SAM/BAM dataset."/> <conditional name="reference_source"> <param name="reference_source_selector" type="select" label="Load reference genome from"> <option value="cached">Local cache</option> <option value="history">History</option> </param> <when value="cached"> <param name="ref_file" type="select" label="Using reference genome" help="REFERENCE_SEQUENCE"> <options from_data_table="all_fasta"> </options> <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> </param> </when> <when value="history"> <param name="ref_file" type="data" format="fasta" label="Use the folloing dataset as the reference sequence" help="REFERENCE_SEQUENCE; You can upload a FASTA sequence to the history and use it as reference" /> </when> </conditional> <param name="window_size" type="integer" value="100" label="The size of windows on the genome that are used to bin reads" help="WINDOW_SIZE; default=100"/> <param name="minimum_genome_fraction" type="float" value="0.00005" label="For summary metrics, exclude GC windows that include less than this fraction of the genome" help="MINIMUM_GENOME_FRACTION; default=0.0005"/> <param name="is_bisulfite_sequenced" type="boolean" label="Calculate the base distribution over PF (passing filtering) reads only" checked="true" truevalue="true" falsevalue="false" help="PF_READS_ONLY"/> <param name="assume_sorted" type="boolean" label="Assume the input file is already sorted" checked="true" truevalue="true" falsevalue="false" help="ASSUME_SORTED"/> <expand macro="VS" /> </inputs> <outputs> <data format="tabular" name="summaryFile" label="${tool.name} on ${on_string}: Summary stats"/> <data format="tabular" name="outFile" label="${tool.name} on ${on_string}: Summary data"/> <data format="pdf" name="pdfFile" label="${tool.name} on ${on_string}: Chart PDF"/> </outputs> <tests> <test> <param name="window_size" value="100" /> <param name="minimum_genome_fraction" value="0.00005" /> <param name="assume_sorted" value="true" /> <param name="is_bisulfite_sequenced" value="true" /> <param name="reference_source_selector" value="history" /> <param name="ref_file" value="picard_CollectGcBiasMetrics_ref.fa" /> <param name="inputFile" value="picard_CollectGcBiasMetrics.bam" ftype="bam" /> <output name="outFile" file="picard_CollectGcBiasMetrics_test1.tab" ftype="tabular" lines_diff="4"/> </test> </tests> <stdio> <exit_code range="1:" level="fatal"/> </stdio> <help> .. class:: infomark **Purpose** Program to chart the nucleotide distribution per cycle in a SAM or BAM file. @dataset_collections@ @description@ ALIGNED_READS_ONLY=Boolean If set to true, calculate the base distribution over aligned reads only. Default value: false. Possible values: {true, false} PF_READS_ONLY=Boolean If set to true calculate the base distribution over PF reads only. Default value: false. This option can be set to 'null' to clear the default value. Possible values: {true, false} ASSUME_SORTED=Boolean AS=Boolean If true (default), then the sort order in the header file will be ignored. Default: True @more_info@ </help> </tool>