Mercurial > repos > devteam > vcfallelicprimitives
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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tool_collections/vcflib/vcfallelicprimitives commit 36e9065027cc7bf721e9d203208477ee88906c57"
author | iuc |
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date | Thu, 23 Jan 2020 08:02:42 -0500 |
parents | a8a4f94aa321 |
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<?xml version="1.0" encoding="utf-8"?> <tool id="vcfallelicprimitives" name="VcfAllelicPrimitives:" version="@WRAPPER_VERSION@+galaxy0"> <description>Split alleleic primitives (gaps or mismatches) into multiple VCF lines</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"></expand> <expand macro="stdio" /> <command> cat '${input}' | vcfallelicprimitives ${m_option} -t '${t_option}' -L "${max_length}" $keep_info $keep_geno > '${out_file1}' </command> <inputs> <param format="vcf" name="input" type="data" label="Select VCF dataset"/> <param name="m_option" type="boolean" checked="false" truevalue="--use-mnps" falsevalue="" label="Retain MNPs as separate events" help="--use-mnps option"/> <param name="t_option" type="text" value="Split primitives" label="Tag records which are split apart of a complex allele with this flag. " help="--tag-parsed option"/> <param name="max_length" type="integer" value="200" label="Do not manipulate records in which either the ALT or REF is longer than (bp)" help="--max-length option"/> <param name="keep_info" type="boolean" truevalue="--keep-info" falsevalue="" checked="False" label="Maintain site and allele-level annotations when decomposing" help="Note that in many cases, such as multisample VCFs, these won't be valid post-decomposition. For biallelic loci in single-sample VCFs, they should be usable with caution. (--keep-info)"/> <param name="keep_geno" type="boolean" truevalue="--keep-geno" falsevalue="" checked="False" label="Maintain genotype-level annotations when decomposing" help="Similar caution should be used for this as for --keep-info. (--keep-geno)"/> </inputs> <outputs> <data format="vcf" name="out_file1" label="${tool.name} on ${on_string}" /> </outputs> <tests> <test> <param name="input" value="vcflib.vcf"/> <output name="out_file1" file="vcfallelicprimitives-test1.vcf"/> </test> </tests> <help> If multiple alleleic primitives (gaps or mismatches) are specified in a single VCF record, this tools splits the record into multiple lines, but drops all INFO fields. "Pure" MNPs are split into multiple SNPs unless the -m flag is provided. Genotypes are phased where complex alleles have been decomposed, provided genotypes in the input. The options are:: -m, --use-mnps Retain MNPs as separate events (default: false). -t, --tag-parsed FLAG Tag records which are split apart of a complex allele with this flag. -L, --max-length LEN Do not manipulate records in which either the ALT or REF is longer than LEN (default: 200). -k, --keep-info Maintain site and allele-level annotations when decomposing. Note that in many cases, such as multisample VCFs, these won't be valid post-decomposition. For biallelic loci in single-sample VCFs, they should be usable with caution. -g, --keep-geno Maintain genotype-level annotations when decomposing. Similar caution should be used for this as for --keep-info. ---- Vcfallelicprimitives @IS_PART_OF_VCFLIB@ </help> <expand macro="citations" /> </tool>