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: Report
Language:unknown
Published: 2015
Subjects:
Online Access:http://hdl.handle.net/10255/dryad.100533
https://doi.org/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.