R/subtyper.R
plinkVariantsDataFrame.Rd
genetic variants data frame from plink data
plinkVariantsDataFrame(rootFileName, targetSNPs, verbose = FALSE)
root for pgen psam and pvar files
snps to extract (optional - if absent, will get all)
boolean
dataframes with both variants and subject ids
Avants BB
# mydf = plinkVariantsDataFrame( fn, c( 'rs6469804', 'rs6859' ) )