Computes intersection between a VCF dataset and a set of genomic intervals defined as either a BED dataset (http://genome.ucsc.edu/FAQ/FAQformat.html#format1) or a manually typed interval (in the form of chr:start-end). |
hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/vcfbedintersect
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
Intersect VCF and BED datasets | 1.0.0_rc1.0 | any |