Mercurial > repos > dfornika > snippy
diff snippy-core.xml @ 2:1a3c85497d96 draft
planemo upload for repository https://github.com/tseemann/snippy commit 73ec6ea773b1b88f7c32a2e8bc57b644b82f7ff9-dirty
author | dfornika |
---|---|
date | Fri, 18 Jan 2019 22:46:34 -0500 |
parents | 0276bb8bd561 |
children | 3f5ced130c5c |
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--- a/snippy-core.xml Fri Jan 18 19:35:46 2019 -0500 +++ b/snippy-core.xml Fri Jan 18 22:46:34 2019 -0500 @@ -9,14 +9,14 @@ <command detect_errors="exit_code"><![CDATA[ perl '$__tool_directory__/snippy_core_wrapper.pl' - '$is_reference' + --ref '$ref' --indirs '${" ".join(map(str, $indirs))}' ]]></command> <inputs> <param name="indirs" type="data" multiple="true" format="zip" label="Snippy input zipped dirs" help="Select all the snippy inputs for alignment" /> - <param name="is_reference" type="boolean" checked="true" truevalue="--noref" falsevalue="" label="Exclude reference" help="Don't include the reference file in the alignment." /> + <param name="ref" type="data" format="fasta,genbank" label="Reference File (either in fasta or genbank format)" help="Fasta or Genbank file to use as the reference" /> <param name="outputs" type="select" multiple="true" display="checkboxes" label="Output selection"> <option value="outaln" selected="True">A core SNP alignment in the fasta format</option> <option value="outfull" selected="False">A whole genome SNP alignment (includes invariant sites)</option> @@ -43,8 +43,8 @@ <tests> <test><!-- Test #1 - test with 2 zipped directories --> - <param name="indirs" value="S1.tgz,S2.tgz" /> - <param name="is_reference" value="false" /> + <param name="indirs" value="S1.tgz,S2.tgz,S3.tgz" /> + <param name="ref" value="GCF_000293905.1_ASM29390v1_genomic.fna" /> <param name="outputs" value="outtxt" /> <output name="alignment_summary" ftype="txt" file="core/core.txt" /> </test>