given an annotated VCF and a BAM file, it genotypes (using the reads in the BAM) each variant in the VCF (for snp or indel) and validates (or not) the 'known' annotation. Outputs a truth table with the PPV and NPV values, and optionally a vcf file with the variants that had enough coverage to be validated. You can optionally provide a minimum depth of coverage and only do the analysis conditional on that. (will write a wiki for this walker, as it might be useful for future validation essays). git-svn-id: file:///humgen/gsa-scr1/gsa-engineering/svn_contents/trunk@5409 348d0f76-0448-11de-a6fe-93d51630548a |
||
|---|---|---|
| R | ||
| analysis/depristo | ||
| archive | ||
| c | ||
| doc | ||
| java | ||
| lua | ||
| matlab | ||
| packages | ||
| perl | ||
| python | ||
| ruby | ||
| scala | ||
| settings | ||
| shell | ||
| testdata | ||
| LICENSE | ||
| build.xml | ||
| ivy.xml | ||