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author | mheinzl |
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date | Wed, 07 Oct 2020 18:48:40 +0000 |
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<?xml version="1.0" encoding="UTF-8"?> <tool id="fasta2fastq" name="FASTA-to-FASTQ" version="1.0.0" profile="19.01"> <description>Convert a FASTA file to a FASTQ file</description> <macros> <import>macros.xml</import> </macros> <command><![CDATA[ python '$__tool_directory__/fasta2fastq.py' -i '$file1' -o '$file2' -s '$score' ]]> </command> <inputs> <param name="file1" type="data" format="fasta" label="FASTA file" optional="false"/> <param name="score" type="integer" label="Quality score" value="40" help="Quality score for each base in all reads. Default = 40."/> </inputs> <outputs> <data name="file2" format="fastq" label="${tool.name} on ${on_string}: FASTQ"/> </outputs> <tests> <test> <param name="file1" value="Reads_in.fasta"/> <output name="file2" file="Reads_out.fastq"/> <param name="score" value="40"/> </test> </tests> <help> <![CDATA[ **What it does** Takes a FASTA file and converts it to a FASTQ file by adding a static quality score. The default quality score for each base in all reads is 40. ]]> </help> <expand macro="citation" /> </tool>