Mercurial > repos > nilesh > vcftools
comparison vcftools.xml @ 12:136a34b6bdfc draft
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author | nilesh |
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date | Wed, 10 Jul 2013 17:47:52 -0400 |
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11:27fd495c6658 | 12:136a34b6bdfc |
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1 <tool id="vcftools" name="VCFtools" version="0.0.1"> | |
2 <description> | |
3 The vcftools program is intended for analysis of diploid SNP data in VCF format. | |
4 </description> | |
5 <requirements> | |
6 <requirement type="package" version="0.1.11">vcftools</requirement> | |
7 </requirements> | |
8 <command> | |
9 vcftools | |
10 | |
11 #if str($basic) == "gzvcf" | |
12 --gzvcf | |
13 #elif str($basic) == "bcf" | |
14 --bcf | |
15 #else | |
16 --vcf | |
17 #end if | |
18 | |
19 $input | |
20 | |
21 #for $chromosome in $chr | |
22 --chr $chromosome.number | |
23 #end for | |
24 | |
25 #for $chromosome in $notchr | |
26 --notchr $chromosome.number | |
27 #end for | |
28 | |
29 #if str($frombp) != "" | |
30 --from-bp $frombp | |
31 #end if | |
32 | |
33 #if str($tobp) != "" | |
34 --to-bp $tobp | |
35 #end if | |
36 | |
37 #for $snp in $snps | |
38 --snp $snp.id | |
39 #end for | |
40 | |
41 #if str(${snpfile.file_name}) != "" | |
42 --snps $snpfile | |
43 #end if | |
44 | |
45 #if str(${excludesnpfile.file_name}) != "" | |
46 --snps $excludesnpfile | |
47 #end if | |
48 | |
49 #if str($indels) == "keeponlyindels" | |
50 --keep-only-indels | |
51 #elif str($indels) == "removeindels" | |
52 --removeindels | |
53 #end if | |
54 | |
55 $removefilterall $recodetostream > out.recode.vcf | |
56 </command> | |
57 <inputs> | |
58 <param name="input" type="data" label="Input vcf file" format="vcf" /> | |
59 <param name="basic" type="select" label="Basic Options" value="vcf"> | |
60 <option value="vcf">Decompressed vcf file (default)</option> | |
61 <option value="gzvcf">Compressed (gzipped) vcf file</option> | |
62 <option value="bcf">Compressed (bgzf) bcf file</option> | |
63 </param> | |
64 <repeat name="chr" title="Include chromosomes to be processed"> | |
65 <param name="number" label="Chromosome number" type="integer" optional="true" /> | |
66 </repeat> | |
67 <repeat name="notchr" title="Exclude chromosomes from processing"> | |
68 <param name="number" label="Chromosome number" type="integer" optional="true" /> | |
69 </repeat> | |
70 <param name="frombp" label="Beginning of range to be processed" help="only if chromosomes are included. You must also specify the end of range to be processed." optional="true" type="integer"/> | |
71 <param name="tobp" label="End of range to be processed" optional="true" type="integer" help="only if chromosomes are included. You must also specify the beginning of range to be processed."/> | |
72 <repeat name="snps" title="SNPs to include"> | |
73 <param name="id" label="ID of SNP" type="text" optional="true" help="e.g. a dbSNP rsID"/> | |
74 </repeat> | |
75 <param name="snpfile" type="data" format="txt, tabular" label="List of SNPs to include" help="The file should contain a list of SNP IDs (e.g. dbSNP rsIDs), with one ID per line." optional="true"/> | |
76 <param name="excludesnpfile" type="data" label = "List of SNPs to disclude" format="txt, tabular" help="The file should contain a list of SNP IDs (e.g. dbSNP rsIDs), with one ID per line." optional="true"/> | |
77 <param name="indels" type="select" label="Indel options" value="none"> | |
78 <option value="keeponlyindels">Keep only indels</option> | |
79 <option value="none">None</option> | |
80 <option value="removeindels"> Remove indels</option> | |
81 </param> | |
82 <param name="removefilterall" type="boolean" truevalue="--remove-filtered-all" falsevalue="" label="Remove all sites with the FILTER tag" value="false" /> | |
83 <param name="recodetostream" type="boolean" truevalue="--recode-to-stream" falsevalue="" label="Recode to stream" value="false" /> | |
84 </inputs> | |
85 <outputs> | |
86 <data format="vcf" name="output" from_work_dir="out.recode.vcf" /> | |
87 </outputs> | |
88 <help> | |
89 Welcome to VCFtools - a program package designed for working with VCF files, such as those generated by the 1000 Genomes Project. The aim of VCFtools is to provide methods for working with VCF files: validating, merging, comparing and calculate some basic population genetic statistics. More information at http://vcftools.sourceforge.net/index.html. | |
90 </help> | |
91 </tool> |