VCF file

This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each variant site identified, we required that >60% of all individuals had 1 or more read at that locus.

Bibliographic Details
Main Authors: Underwood, Zachary E., Mandeville, Elizabeth G., Walters, Annika W.
Format: Dataset
Language:unknown
Published: Dryad Digital Repository 2015
Subjects:
USA
Online Access:https://dx.doi.org/10.5061/dryad.7842r/2
http://datadryad.org/resource/doi:10.5061/dryad.7842r/2
Description
Summary:This is a .vcf file produced by calling variant genetic sites using samtools and bcftools. For each variant site identified, we required that >60% of all individuals had 1 or more read at that locus.