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    To learn how to use VCFtools to filter a VCF file for missing data, genotype depth, locus quality score, minor allele frequency, and genotype call depth · To
    Some of the commands in VCFtools require that you operate on a compressed VCF file. Given file mydata.vcf, in the online VCFtools manual.
    A set of tools written in Perl and C++ for working with VCF files. Home · Documentation · Download ZIP · Download TAR · View On GitHub. NAME SYNOPSIS
    VCFtools expects files in VCF format v4.0, v4.1 or v4.2. Further details of these files can be found in the PLINK documentation.
    vcftools is a suite of functions for use on genetic variation data in the form of VCF and BCF files. The tools provided will be used mainly to summarize data,
    Vcftools. Version: 0.1.16. A set of tools written in Perl and C++ for working with VCF files The manual is on the web at the original home pageManual Outline · Ancestry Informative Markers · VCF summary information · Genetic Relationship Matrix · Filter data fields in a VCF file · Convert genotype/haplotype

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