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Extract VCF information
extractCoverageFromVcf(filename, samplename)
A dataframe list with members of haplotypes, proportions and log likelihood of the MCMC chain.
CHROM SNP chromosomes.
CHROM
POS SNP positions.
POS
refCount reference allele count.
refCount
altCount alternative allele count.
altCount
VCF file name.
Sample name
extractCoverageFromVcf
extractCoverageFromTxt
vcfFile = system.file("extdata", "PG0390-C.test.vcf.gz", package = "DEploid.utils") vcf = extractCoverageFromVcf(vcfFile, "PG0390-C")
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