FxSKAT.zip folder containing the R code and an example data file.
PURPOSE:
The R code provided is for detecting associations between rare and common variants in the X chromosome and complex diseases using family data. The code may also be used for analyzing variants in the autosomes.
The folder may be downloaded from the link below
FxSKAT.zip folder containing the R code and an example data file.
If you have any questions, please email Asuman Turkmen (turkmen@stat.osu.edu) or Shili Lin (shili@stat.osu.edu).