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Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
Learning the Variant Call Format
A command-line parser for VCF files designed for population genetics analyses.
Checks vcf files and removes loci and samples with too many missings, can also input genotypes in missing (various options for this).
Modify KASP assay calls to a VCF format