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Computes genotype frequencies from the sequencing data with a vcf type of the 1000 Genomes Project.
geno.freq(genoG)
matrix of haplotypes. Each row indicates a variant, and each column ind icates a haplotype of an individual. Two alleles of 0 and 1 are available.
matrix of genotype frequencies of each variant.
# NOT RUN { data(apoeG) geno.freq(apoeG) # }
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