Mercurial > repos > iuc > delly_call
view macros.xml @ 0:36772204dee5 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit 86ada42b811af0262618636f2d8d1788274f9884"
author | iuc |
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date | Mon, 28 Sep 2020 07:45:21 +0000 |
parents | |
children | 53d90d86fc83 |
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<?xml version="1.0"?> <macros> <token name="@TOOL_VERSION@">0.8.3</token> <token name="@DESCRIPTION@"></token> <xml name="requirements"> <requirements> <requirement type="package" version="@TOOL_VERSION@">delly</requirement> <requirement type="package" version="1.10.2">bcftools</requirement> </requirements> </xml> <xml name="version_command"> <version_command><![CDATA[delly -v 2>&1 | grep 'Delly version' | cut -f 3 -d ' ']]></version_command> </xml> <xml name="citations"> <citations> <citation type="doi">10.1093/bioinformatics/bts378</citation> </citations> </xml> <!-- input --> <xml name="exclude"> <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/> </xml> <xml name="genome"> <param argument="--genome" type="data" format="fasta" label="Select genome"/> </xml> <xml name="genoqual"> <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/> </xml> <xml name="minclip"> <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/> </xml> <xml name="maxreadsep"> <param argument="--maxreadsep" type="integer" value="40" label="Set maximum read separation"/> </xml> <xml name="minrefsep"> <param argument="--minrefsep" type="integer" value="25" label="Set minimum reference separation"/> </xml> <xml name="samples" token_format="bam" token_multiple="true" token_label="Select sample file(s)"> <param name="samples" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/> </xml> <xml name="svtype"> <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect"> <option value="ALL" selected="true">All types (ALL)</option> <option value="DEL">Deletion (DEL)</option> <option value="INS">Insertion (INS)</option> <option value="DUP">Duplication (DUP)</option> <option value="INV">Inversion (INV)</option> <option value="BND">Translocation (BND)</option> </param> </xml> <xml name="vcffile"> <param argument="--vcffile" type="data" format="vcf,bcf" optional="true" label="Select genotyping file"/> </xml> <!-- output --> <xml name="vcf"> <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)"> <filter>'vcf' in oo['out']</filter> </data> </xml> <xml name="bcf"> <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)"> <filter>'bcf' in oo['out']</filter> </data> </xml> <xml name="dump"> <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads"> <filter>'dump' in oo['out']</filter> </data> </xml> <xml name="log"> <data name="out_log" format="txt" from_work_dir="log.txt" label="${tool.name} on ${on_string}: Log"> <filter>'log' in oo['out']</filter> </data> </xml> <!-- Help --> <token name="@WID@"><![CDATA[ Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome. ]]></token> <token name="@REFERENCES@"><![CDATA[ More information are available on `github <https://github.com/dellytools/delly>`_. ]]></token> </macros>