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view bcftools_convert_from_vcf.xml @ 4:8714c1caa3ee draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/bcftools commit 3edcac645f34d5a94884dedaf95c5774f4afc5c7
author | iuc |
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date | Sat, 11 Mar 2017 17:58:33 -0500 |
parents | 16f221807ecd |
children | 2c5a7bd98c81 |
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<?xml version='1.0' encoding='utf-8'?> <tool name="bcftools @EXECUTABLE@ from vcf" id="bcftools_@EXECUTABLE@_from_vcf" version="@VERSION@"> <description>Converts VCF/BCF to IMPUTE2/SHAPEIT formats</description> <macros> <token name="@EXECUTABLE@">convert</token> <import>macros.xml</import> <xml name="macro_vcf_ids"> <param name="vcf_ids" type="boolean" truevalue="--vcf-ids" falsevalue="" checked="false" label="Output VCF IDs instead of CHROM:POS_REF_ALT" help="(\-\-vcf_ids)"/> </xml> <xml name="macro_haploid2diploid"> <param name="haploid2diploid" type="boolean" truevalue="--haploid2diploid" falsevalue="" checked="false" label="convert haploid genotypes to diploid homozygotes" help="(\-\-haploid2diploid)"/> </xml> </macros> <expand macro="requirements" /> <expand macro="version_command" /> <command detect_errors="aggressive"><![CDATA[ @PREPARE_ENV@ @PREPARE_INPUT_FILE@ #set $section = $sec_restrict @PREPARE_TARGETS_FILE@ bcftools @EXECUTABLE@ #if $convert.convert_to == 'gen_sample': --tag $convert.tag $convert.chrom $convert.vcf_ids --gensample "$output_gen,$output_samples" #elif $convert.convert_to == 'hap_sample': $convert.vcf_ids $convert.haploid2diploid --hapsample "$output_hap,$output_samples" #elif $convert.convert_to == 'hap_legend_sample': $convert.vcf_ids $convert.haploid2diploid --haplegendsample "$output_hap,$output_legend,$output_samples" #end if ## VCF input section #set $section = $sec_restrict @INCLUDE@ @EXCLUDE@ @REGIONS@ @TARGETS@ @SAMPLES@ ## Primary Input/Outputs "$input_file" . ]]> </command> <inputs> <expand macro="macro_input" /> <section name="sec_restrict" expanded="false" title="Restrict to"> <expand macro="macro_regions" /> <expand macro="macro_targets" /> <expand macro="macro_samples" /> <expand macro="macro_include" /> <expand macro="macro_exclude" /> </section> <conditional name="convert"> <param name="convert_to" type="select" label="convert to"> <option value="gen_sample">gen sample - IMPUTE2 or SHAPEIT</option> <option value="hap_sample">hap sample - IMPUTE2 or SHAPEIT</option> <option value="hap_legend_sample">hap legend sample - IMPUTE2 or SHAPEIT</option> </param> <when value="gen_sample"> <param name="tag" type="select" label="tag to take values for .gen file: GT,PL,GL,GP"> <option value="GT">GT</option> <option value="PL">PL</option> <option value="GP">GP</option> <!-- <option value="GL">GL</option> --> </param> <param name="chrom" type="boolean" truevalue="--chrom" falsevalue="" checked="false" label="Output chromosome in first column instead of CHROM:POS_REF_ALT" help="(\-\-chrom)"/> <expand macro="macro_vcf_ids"/> </when> <when value="hap_sample"> <expand macro="macro_haploid2diploid"/> <expand macro="macro_vcf_ids"/> </when> <when value="hap_legend_sample"> <expand macro="macro_haploid2diploid"/> <expand macro="macro_vcf_ids"/> </when> </conditional> </inputs> <outputs> <data name="output_gen" format="tabular" label="${input_file.name.rsplit('.',1)[0]}.gen"> <filter>convert['convert_to'] == 'gen_sample'</filter> </data> <data name="output_hap" format="tabular" label="${input_file.name.rsplit('.',1)[0]}.haps"> <filter>convert['convert_to'] in ('hap_sample','hap_legend_sample')</filter> </data> <data name="output_legend" format="tabular" label="${input_file.name.rsplit('.',1)[0]}.legend"> <filter>convert['convert_to'] == 'hap_legend_sample'</filter> </data> <data name="output_samples" format="tabular" label="${input_file.name.rsplit('.',1)[0]}.samples"/> </outputs> <tests> <test> <param name="input_file" ftype="vcf" value="convert.vcf" /> <param name="convert_to" value="gen_sample" /> <output name="output_gen"> <assert_contents> <has_text text="X:2698560_G_A X:2698560_G_A 2698560 G A 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0 1 0 0"/> </assert_contents> </output> <output name="output_samples"> <assert_contents> <has_text text="NA00001 NA00001 0"/> </assert_contents> </output> </test> <test> <param name="input_file" ftype="vcf" value="convert.vcf" /> <param name="convert_to" value="gen_sample" /> <param name="tag" value="GP" /> <param name="chrom" value="True" /> <output name="output_gen"> <assert_contents> <has_text text="X X:2698560_G_A 2698560 G A 1.00"/> </assert_contents> </output> </test> <test> <param name="input_file" ftype="vcf" value="check.vcf" /> <param name="convert_to" value="gen_sample" /> <param name="tag" value="GT" /> <param name="chrom" value="True" /> <param name="vcf_ids" value="True" /> <output name="output_gen"> <assert_contents> <has_text text="1 id3D 3062915 GTTT G 0 1 0 0 1 0"/> </assert_contents> </output> </test> <test> <param name="input_file" ftype="vcf" value="convert.vcf" /> <param name="convert_to" value="hap_sample" /> <output name="output_hap"> <assert_contents> <has_text text="X X:2698769_AAG_A 2698769 AAG A 1 0 1 1 0 1 1 0 1 0 0 0 0 0 0 0 0 0 0 0"/> </assert_contents> </output> </test> <test> <param name="input_file" ftype="vcf" value="convert.vcf" /> <param name="convert_to" value="hap_legend_sample" /> <output name="output_hap"> <assert_contents> <has_text text="1 0 1 1 0 1 1 0 1 0 0 0 0 0 0 0 0 0 0 0"/> </assert_contents> </output> <output name="output_legend"> <assert_contents> <has_text text="X:2698769_AAG_A 2698769 AAG A"/> </assert_contents> </output> <output name="output_samples"> <assert_contents> <has_text text="sample population group sex"/> <has_text text="NA00001 NA00001 NA00001 2"/> </assert_contents> </output> </test> </tests> <help><![CDATA[ ===================================== bcftools @EXECUTABLE@ from vcf ===================================== Converts VCF/BCF to other formats. See man page for file formats details. @REGIONS_HELP@ @TARGETS_HELP@ @EXPRESSIONS_HELP@ @BCFTOOLS_MANPAGE@#@EXECUTABLE@ @BCFTOOLS_WIKI@ ]]> </help> <expand macro="citations" /> </tool>