Description Usage Arguments Value
View source: R/sim_StudySeqFunctions.R
Remove any markers for which all founders, in the study, are homozygous for the wild-type allele. Since we do not model de novo mutations, it is not possible for non-founders to develop mutations at these loci.
1 | remove_allWild(f_haps, SNV_map)
|
f_haps |
The founder haplotypes data. This is a list of family lists. By family, this contains the haplotypes for each founder (first item), and a list of ID numbers (second item) which is used to map the haplotype to the person to whom it belongs. |
SNV_map |
data.frame. Catalogs the SNV data contained in the familial haplotypes. |
A list (by family) of haplotype matrices and ID vectors and the reduce marker data set.
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