ReadList {pgenlibr} | R Documentation |
Load dosages for multiple variants as a numeric matrix.
Description
This function treats the data as diploid; divide by 2 to obtain haploid dosages.
Usage
ReadList(pgen, variant_subset, meanimpute = FALSE)
Arguments
pgen |
Object returned by NewPgen(). |
variant_subset |
Integer vector containing 1-based indexes of variants to load. |
meanimpute |
Optional; if true, missing values are mean-imputed instead of being represented by NA. |
Value
Numeric matrix, where rows correspond to samples, and columns correspond to variant_subset. Values are in [0, 2] indicating ALT allele dosages, or NA for missing dosages. For multiallelic variants, all ALT alelles are combined.
[Package pgenlibr version 0.3.7 Index]