0
|
1 <tool id="vcfannotategenotypes" name="VCFannotateGenotypes:" version="0.0.1">
|
|
2 <requirements>
|
|
3 <requirement type="package" version="586c5ae5d57a38dae6b32ea831fb1f7cfa14c9bd">vcflib</requirement>
|
|
4 </requirements>
|
|
5 <description>Annotate genotypes in a VCF dataset using genotypes from another VCF dataset</description>
|
|
6 <command>vcfannotategenotypes "${tag_option}" "${input1}" "${input2}" > "${out_file1}"</command>
|
|
7 <inputs>
|
|
8 <param format="vcf" name="input1" type="data" label="Annotate genotypes in" help="First VCF dataset"/>
|
|
9 <param format="vcf" name="input2" type="data" label="using genotypes from" help="Second VCF dataset"/>
|
|
10 <param name="tag_option" size="20" type="text" value="added-genotypes" label="Mark genotypes added to the first dataset with this tag" help="Annotation tag"/>
|
|
11 </inputs>
|
|
12 <outputs>
|
|
13 <data format="vcf" name="out_file1" />
|
|
14 </outputs>
|
|
15 <tests>
|
|
16 <test>
|
|
17 <param name="tag_option" value="added-genotypes"/>
|
|
18 <param name="input1" value="vcflib.vcf"/>
|
|
19 <param name="input2" value="vcfannotategenotypes-input2.vcf"/>
|
|
20 <output name="out_file1" file="vcfannotategenotypes-test1.vcf" />
|
|
21 </test>
|
|
22 </tests>
|
|
23 <help>
|
|
24
|
|
25 Annotates genotypes in the **First** file with genotypes in the **Second** adding the genotype as another flag to each sample filed in the first file. **Annotation-tag** is the name of the sample flag which is added to store the annotation. also adds a 'has\_variant' flag for sites where the second file has a variant.
|
|
26
|
|
27 -----
|
|
28
|
|
29 Vcfannotate is a part of VCFlib toolkit developed by Erik Garrison (https://github.com/ekg/vcflib).
|
|
30
|
|
31
|
|
32 </help>
|
|
33 </tool>
|