Mercurial > repos > dereeper > sniplay
diff SNP_density/calculateSlidingWindowsSNPdensitiesFromVCF_wrapper.xml @ 10:c6640c49fd01 draft
planemo upload commit 475f4d7d8442a0d75e103af326ae5881c4d2a4ac
author | dereeper |
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date | Mon, 16 Apr 2018 09:00:24 -0400 |
parents | 98c37a5d67f4 |
children |
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--- a/SNP_density/calculateSlidingWindowsSNPdensitiesFromVCF_wrapper.xml Wed Feb 07 22:08:47 2018 -0500 +++ b/SNP_density/calculateSlidingWindowsSNPdensitiesFromVCF_wrapper.xml Mon Apr 16 09:00:24 2018 -0400 @@ -3,7 +3,6 @@ <!-- [REQUIRED] Tool description displayed after the tool name --> <description> Calculate SNP densities along chromosome from a VCF input</description> - <!-- [OPTIONAL] 3rd party tools, binaries, modules... required for the tool to work --> <requirements> <requirement type="binary">perl</requirement> @@ -58,7 +57,7 @@ </tests> <!-- [OPTIONAL] Help displayed in Galaxy --> - <help> + <help><![CDATA[ .. class:: infomark @@ -66,19 +65,16 @@ | **Please cite** "SNiPlay3: a web-based application for exploration and large scale analyses of genomic variations", **Dereeper A. et al.**, Nucl. Acids Res. (1 july 2015) 43 (W1). +.. class:: infomark + +**Galaxy integration** Provided by Southgreen & Andres Gwendoline (Institut Français de Bioinformatique) & Marcon Valentin (IFB & INRA) .. class:: infomark -**Galaxy integration** Andres Gwendoline, Institut Français de Bioinformatique. - -.. class:: infomark - -**Support** For any questions about Galaxy integration, please send an e-mail to support.abims@sb-roscoff.fr +**Support** For any questions about Galaxy integration, please send an e-mail to alexis.dereeper@ird.fr --------------------------------------------------- - - ============= SNP densities ============= @@ -89,18 +85,19 @@ Calculate SNP densities along chromosome from a VCF file - ------------------ -Workflow position ------------------ +------------ +Dependencies +------------ +VCFtools + vcftools_ 0.1.14, Conda version +VCFtools Perl libraries + perl-vcftools-vcf_ 0.1.14, Conda version +Bioperl + perl-bioperl_ 1.6.924, Conda version -**Upstream tool** - -=============== ====================== =========== -Name output file(s) format -=============== ====================== =========== -=============== ====================== =========== - +.. _vcftools: https://anaconda.org/bioconda/vcftools +.. _perl-vcftools-vcf: https://anaconda.org/bioconda/perl-vcftools-vcf +.. _perl-bioperl: https://anaconda.org/bioconda/perl-bioperl ---------- Input file @@ -109,7 +106,6 @@ VCF file File with SNPs - ---------- Parameters ---------- @@ -120,7 +116,6 @@ Output name Output base name for the two ouput files - ------------ Output files ------------ @@ -130,7 +125,6 @@ Output_name.by_sample Tabular file with SNP density for each sample - --------------------------------------------------- @@ -138,8 +132,8 @@ Working example --------------- -Input files -=========== +Input file +========== vcf file ----------- @@ -187,7 +181,7 @@ chr1 43 43 40 chr1 139 167 141 - </help> + ]]></help> <citations> <!-- [HELP] As DOI or BibTex entry --> <citation type="bibtex">@article{Dereeper03062015,