MVP.Data.VCF2MVP | R Documentation |
Accept the | or / separated markers, any variant sites that are not 0 or 1 will be considered NA.
MVP.Data.VCF2MVP(
vcf_file,
out = "mvp",
maxLine = 10000,
type.geno = "char",
threads = 1,
verbose = TRUE
)
vcf_file |
Genotype in VCF format |
out |
the name of output file |
maxLine |
the number of markers handled at a time, smaller value would reduce the memory cost |
type.geno |
the type of genotype elements |
threads |
number of thread for transforming |
verbose |
whether to print the reminder |
number of individuals and markers. Output files: genotype.desc, genotype.bin: genotype file in bigmemory format phenotype.phe: ordered phenotype file, same taxa order with genotype file map.map: SNP information
vcfPath <- system.file("extdata", "01_vcf", "mvp.vcf", package = "rMVP")
MVP.Data.VCF2MVP(vcfPath, tempfile("outfile"), threads=1)
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