Mercurial > repos > devteam > vcfflatten
diff vcfflatten.xml @ 1:1336a70f5c02 draft
planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/vcflib/vcfflatten commit 0b9b6512272b82637c2f1e831367e89aed77ae79
| author | devteam |
|---|---|
| date | Thu, 15 Sep 2016 16:06:16 -0400 |
| parents | 38d93ca9c0f0 |
| children | b24e368ae7b1 |
line wrap: on
line diff
--- a/vcfflatten.xml Thu Mar 19 14:31:30 2015 -0400 +++ b/vcfflatten.xml Thu Sep 15 16:06:16 2016 -0400 @@ -1,30 +1,30 @@ -<tool id="vcfflatten2" name="VCFflatten:" version="0.0.3"> - <description>Removes multi-allelic sites by picking the most common alternate</description> - <macros> - <import>macros.xml</import> - </macros> - <expand macro="requirements"></expand> - <expand macro="stdio" /> - <command>vcfflatten "${input1}" > "${out_file1}"</command> - <inputs> - <param format="vcf" name="input1" type="data" label="Select VCF dataset"/> - </inputs> - <outputs> - <data format="vcf" name="out_file1" /> - </outputs> - <tests> - <test> - <param name="input1" value="vcfflatten-input1.vcf"/> - <output name="out_file1" file="vcfflatten-test1.vcf"/> - </test> - </tests> - <help> - -Removes multi-allelic sites by picking the most common alternate. Requires allele frequency specification 'AF' and use of 'G' and 'A' to specify the fields which vary according to the Allele or Genotype. - ----- - -Vcfflatten @IS_PART_OF_VCFLIB@ -</help> - <expand macro="citations" /> -</tool> +<tool id="vcfflatten2" name="VCFflatten:" version="@WRAPPER_VERSION@.0"> + <description>Removes multi-allelic sites by picking the most common alternate</description> + <macros> + <import>macros.xml</import> + </macros> + <expand macro="requirements"/> + <expand macro="stdio" /> + <command>vcfflatten "${input1}" > "${out_file1}"</command> + <inputs> + <param format="vcf" name="input1" type="data" label="Select VCF dataset"/> + </inputs> + <outputs> + <data format="vcf" name="out_file1" /> + </outputs> + <tests> + <test> + <param name="input1" value="vcfflatten-input1.vcf"/> + <output name="out_file1" file="vcfflatten-test1.vcf"/> + </test> + </tests> + <help> + +Removes multi-allelic sites by picking the most common alternate. Requires allele frequency specification 'AF' and use of 'G' and 'A' to specify the fields which vary according to the Allele or Genotype. + +---- + +Vcfflatten @IS_PART_OF_VCFLIB@ +</help> + <expand macro="citations" /> +</tool>