Mercurial > repos > devteam > picard
diff picard_CollectGcBiasMetrics.xml @ 33:3f254c5ced1d draft default tip
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/picard commit 9ecbbb878d68a980ba35a90865e524c723ca3ed8
author | iuc |
---|---|
date | Sun, 03 Mar 2024 16:06:11 +0000 |
parents | f9242e01365a |
children |
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--- a/picard_CollectGcBiasMetrics.xml Mon Sep 25 08:32:17 2023 +0000 +++ b/picard_CollectGcBiasMetrics.xml Sun Mar 03 16:06:11 2024 +0000 @@ -1,13 +1,12 @@ -<tool name="CollectGcBiasMetrics" id="picard_CollectGcBiasMetrics" version="@TOOL_VERSION@.@WRAPPER_VERSION@"> - <description>charts the GC bias metrics</description> - <macros> - <import>picard_macros.xml</import> - <token name="@WRAPPER_VERSION@">1</token> - </macros> - <expand macro="requirements"> - <requirement type="package" version="3.4.1">r-base</requirement> +<tool name="CollectGcBiasMetrics" id="picard_CollectGcBiasMetrics" version="@TOOL_VERSION@.@WRAPPER_VERSION@" profile="@PROFILE@"> + <description>charts the GC bias metrics</description> + <macros> + <import>picard_macros.xml</import> + <token name="@WRAPPER_VERSION@">0</token> + </macros> + <expand macro="requirements"> </expand> - <command detect_errors="exit_code"><![CDATA[ + <command detect_errors="exit_code"><![CDATA[ @java_options@ @symlink_element_identifier@ ##set up input files @@ -16,71 +15,64 @@ @handle_reference_source@ - picard - CollectGcBiasMetrics - INPUT='$escaped_element_identifier' - OUTPUT="${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="${assume_sorted}" + picard CollectGcBiasMetrics + --INPUT '$escaped_element_identifier' + --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="${validation_stringency}" - QUIET=true - VERBOSITY=ERROR + --VALIDATION_STRINGENCY '${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"> + <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 ${on_string}: Chart PDF"/> - </outputs> - - <tests> - <test> - <param name="window_size" value="100" /> - <param name="minimum_genome_fraction" value="0.00005" /> - <param name="assume_sorted" value="true" /> - <param name="is_bisulfite_sequenced" value="true" /> - <param name="reference_source_selector" value="history" /> - <param name="ref_file" value="picard_CollectGcBiasMetrics_ref.fa" /> - <param name="inputFile" value="picard_CollectGcBiasMetrics.bam" ftype="bam" /> - <output name="outFile" file="picard_CollectGcBiasMetrics_test1.tab" ftype="tabular" lines_diff="4"/> - </test> - </tests> - - - <help> + <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/> + </param> + </when> + <when value="history"> + <param name="ref_file" type="data" format="fasta" label="Use the folloing dataset as the reference sequence" help="REFERENCE_SEQUENCE; You can upload a FASTA sequence to the history and use it as reference"/> + </when> + </conditional> + <param name="window_size" type="integer" value="100" label="The size of windows on the genome that are used to bin reads" help="WINDOW_SIZE; default=100"/> + <param name="minimum_genome_fraction" type="float" value="0.00005" label="For summary metrics, exclude GC windows that include less than this fraction of the genome" help="MINIMUM_GENOME_FRACTION; default=0.0005"/> + <param name="is_bisulfite_sequenced" type="boolean" label="Calculate the base distribution over PF (passing filtering) reads only" checked="true" truevalue="true" falsevalue="false" help="PF_READS_ONLY"/> + <param name="assume_sorted" type="boolean" label="Assume the input file is already sorted" checked="true" truevalue="true" falsevalue="false" help="ASSUME_SORTED"/> + <expand macro="VS"/> + </inputs> + <outputs> + <data format="tabular" name="summaryFile" label="${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> + <help> .. class:: infomark @@ -105,5 +97,5 @@ @more_info@ </help> - <expand macro="citations" /> + <expand macro="citations"/> </tool>