Mercurial > repos > wolma > mimodd
diff vcf_filter.xml @ 5:bdd1995c9e66
upgrade to mimodd version 0.1.6.1
author | Wolfgang Maier |
---|---|
date | Tue, 28 Jul 2015 23:21:11 +0200 |
parents | ffee8534a5c4 |
children | 85214e4428fd |
line wrap: on
line diff
--- a/vcf_filter.xml Thu Jun 04 17:52:04 2015 +0200 +++ b/vcf_filter.xml Tue Jul 28 23:21:11 2015 +0200 @@ -1,4 +1,4 @@ -<tool id="vcf_filter" name="VCF Filter"> +<tool id="vcf_filter" name="VCF Filter" version="0.1.6.1"> <description>Extracts lines from a vcf variant file based on field-specific filters</description> <macros> <import>toolshed_macros.xml</import> @@ -28,6 +28,10 @@ #for $i in $datasets "$i.GQ" #end for + --af + #for $i in $datasets + "#echo ($i.AF or "::")#" + #end for #end if #if len($regions): -r @@ -54,6 +58,7 @@ <param name="GT" type="text" label="genotype pattern(s) for the inclusion of variants" help="keep only variants for which the genotype of the sample matches the specified pattern; format: x/x where x = 0 is wildtype and x = 1 is mutant. Multiple genotypes can be specified as a comma-separated list." /> <param name="DP" type="integer" label="depth of coverage for the sample at the variant site" value = "0" help="keep only variants with at least this sample-specific coverage at the variant site" /> <param name="GQ" type="integer" label="genotype quality for the variant in the sample" value = "0" help="keep only variants for which the genotype prediction for the sample has at least this quality" /> + <param name="AF" type="text" label="allelic fraction filter" help="expected format: [allele number]:[minimal fraction]:[maximal fraction]; keep only variants for which the fraction of sample-specific reads supporting a given allele number is between minimal and maximal fraction; if allele number is omitted, the filter operates on the most frequent non-reference allele instead" /> </repeat> <repeat name="regions" title="Region Filter" default="0" min="0" help = "Filter variant sites by their position in the genome. If multiple Region Filters are specified, all variants that fall in ONE of the regions are reported."> <param name="chrom" type="text" label="Chromosome" />