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.
Main Authors: | , , |
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Format: | Report |
Language: | unknown |
Published: |
2015
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Subjects: | |
Online Access: | http://hdl.handle.net/10255/dryad.100533 https://doi.org/10.5061/dryad.7842r/2 |
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. |
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