Mercurial > repos > mheinzl > variant_analyzer2
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planemo upload for repository https://github.com/Single-Molecule-Genetics/VariantAnalyzerGalaxy/tree/master/tools/variant_analyzer commit ee4a8e6cf290e6c8a4d55f9cd2839d60ab3b11c8
author | mheinzl |
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date | Mon, 22 Feb 2021 16:31:04 +0000 |
parents | 84a1a3f70407 |
children | d21960b45a6b |
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<?xml version="1.0" encoding="UTF-8"?> <tool id="mut2sscs" name="DCS mutations to SSCS stats:" version="2.0.1" profile="19.01"> <description>Extracts all tags from the single stranded consensus sequence (SSCS) bam file that carry a mutation at the same position a mutation is called in the duplex consensus sequence (DCS) and calculates their frequencies</description> <macros> <import>va_macros.xml</import> </macros> <expand macro="requirements"/> <command><![CDATA[ ln -s '$file2' bam_input.bam && ln -s '${file2.metadata.bam_index}' bam_input.bam.bai && python '$__tool_directory__/mut2sscs.py' --mutFile '$file1' --bamFile bam_input.bam --outputJson '$output_json' ]]> </command> <inputs> <param name="file1" type="data" format="vcf" label="DCS Mutation File" optional="false" help="VCF file with DCS mutations. See Help section below for a detailed explanation."/> <param name="file2" type="data" format="bam" label="SSCS BAM File" optional="false" help="BAM file with aligned SSCS reads."/> </inputs> <outputs> <data name="output_json" format="json" label="${tool.name} on ${on_string}: JSON"/> </outputs> <tests> <test> <param name="file1" value="FreeBayes_test.vcf"/> <param name="file2" value="SSCS_test.bam"/> <output name="output_json" file="SSCS_counts_test.json" lines_diff="2"/> </test> </tests> <help> <![CDATA[ **What it does** Takes a VCF file with DCS mutations and a BAM file of aligned SSCS reads as input and writes statistics about tags of reads that carry a mutation in the SSCS at the same position a mutation is called in the DCS to a user specified output file.. **Input** **Dataset 1:** VCF file with duplex consesus sequence (DCS) mutations. E.g. generated by the `FreeBayes variant caller <https://arxiv.org/abs/1207.3907>`_. **Dataset 2:** BAM file of aligned single stranded consensus sequence (SSCS) reads. This file can be obtained by the tool `Map with BWA-MEM <https://arxiv.org/abs/1303.3997>`_. **Output** The output is a json file containing dictonaries with stats of tags that carry a mutation in the SSCS at the same position a mutation is called in the DCS. ]]> </help> <expand macro="citation" /> </tool>