Mercurial > repos > artbio > snvtocnv
changeset 2:e0724d649885 draft default tip
planemo upload for repository https://github.com/ARTbio/tools-artbio/tree/master/tools/snvtocnv commit 116f2555558a283190cd1dd60ee25b359bcda51e
author | artbio |
---|---|
date | Fri, 20 May 2022 17:07:54 +0000 |
parents | d2833cfb3f08 |
children | |
files | sequenza_index.xml snvtocnv.xml |
diffstat | 2 files changed, 8 insertions(+), 8 deletions(-) [+] |
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--- a/sequenza_index.xml Thu May 19 20:35:24 2022 +0000 +++ b/sequenza_index.xml Fri May 20 17:07:54 2022 +0000 @@ -1,4 +1,4 @@ -<tool id="sequenzaindex" name="create GC_wiggle of reference genome" version="0.7.0"> +<tool id="sequenzaindex" name="create GC_wiggle of reference genome" version="3.0.0+galaxy1"> <description> </description> <macros> @@ -20,18 +20,18 @@ <param name="window" type="integer" value="50" label="window size" help="The size of the wiggle for GC content calculation" /> </inputs> <outputs> - <data name="refwig" format="txt" label="reference_wig" /> + <data name="refwig" format="wig" label="reference_wig" /> </outputs> <tests> <test> <param name="window" value="100" ftype="vcf" /> <param name="reference" value="hg19_chr22.fa.gz" /> - <output name="refwig" file="hg19.GCref.txt" ftype="txt" /> + <output name="refwig" file="hg19.GCref.txt" ftype="wig" /> </test> <test> <param name="window" value="100" ftype="vcf" /> <param name="reference" value="hg38_chr22.fa.gz" /> - <output name="refwig" file="hg38.GCref.txt" ftype="txt" /> + <output name="refwig" file="hg38.GCref.txt" ftype="wig" /> </test> </tests>
--- a/snvtocnv.xml Thu May 19 20:35:24 2022 +0000 +++ b/snvtocnv.xml Fri May 20 17:07:54 2022 +0000 @@ -1,4 +1,4 @@ -<tool id="snvtocnv" name="Infer CNVs from SNVs" version="3.0.0+galaxy0"> +<tool id="snvtocnv" name="Infer CNVs from SNVs" version="3.0.0+galaxy1"> <description> </description> <macros> @@ -34,9 +34,9 @@ <param name="input_snvs" type="data" format="vcf" label="SNVs to process in a vcf file"/> </inputs> <outputs> - <data name="wiggle" format="txt" label="binned wiggle" /> - <data name="sample_segment" format="txt" label="sample segments" from_work_dir="test/sample_segments.txt" /> - <data name="alt_solutions" format="txt" label="alternate solutions" from_work_dir="test/sample_alternative_solutions.txt" /> + <data name="wiggle" format="wig" label="binned wiggle" /> + <data name="sample_segment" format="tabular" label="sample segments" from_work_dir="test/sample_segments.txt" /> + <data name="alt_solutions" format="tabular" label="alternate solutions" from_work_dir="test/sample_alternative_solutions.txt" /> <data name="cnvs" format="tabular" label="Annotated CNVs" /> <data name="chrom_depths" format="pdf" label="Chromosomes sequencing depth" from_work_dir="test/sample_chromosome_depths.pdf"/> <data name="chrom_view" format="pdf" label="Chromosomes views" from_work_dir="test/sample_chromosome_view.pdf"/>