# HG changeset patch # User nilesh # Date 1373492872 14400 # Node ID 136a34b6bdfc1b46cc6d7d5b14a9d67a659369b5 # Parent 27fd495c66589cef6eb3de866f21ec159d25e971 Uploaded diff -r 27fd495c6658 -r 136a34b6bdfc vcftools.xml --- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/vcftools.xml Wed Jul 10 17:47:52 2013 -0400 @@ -0,0 +1,91 @@ + + + The vcftools program is intended for analysis of diploid SNP data in VCF format. + + + vcftools + + + vcftools + + #if str($basic) == "gzvcf" + --gzvcf + #elif str($basic) == "bcf" + --bcf + #else + --vcf + #end if + + $input + + #for $chromosome in $chr + --chr $chromosome.number + #end for + + #for $chromosome in $notchr + --notchr $chromosome.number + #end for + + #if str($frombp) != "" + --from-bp $frombp + #end if + + #if str($tobp) != "" + --to-bp $tobp + #end if + + #for $snp in $snps + --snp $snp.id + #end for + + #if str(${snpfile.file_name}) != "" + --snps $snpfile + #end if + + #if str(${excludesnpfile.file_name}) != "" + --snps $excludesnpfile + #end if + + #if str($indels) == "keeponlyindels" + --keep-only-indels + #elif str($indels) == "removeindels" + --removeindels + #end if + + $removefilterall $recodetostream > out.recode.vcf + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + + 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. + + \ No newline at end of file