Dear All,
I have Binary version of Plink BED file with variants from all chromosomes and of different individuals from multiple populations around the globe. I want to Perform LD pruning using Plink-1.9, with following parameters:
./plink --indep-pairwise 1000 50 0.2
//here's 1000 is windows size, 50 is step size and 0.2 is r^2 threshold.
My questions is:
1. Should i have to split my file into different chromosomes, like chr1, chr2 and later perform LD pruning or is that Plink can handle variants data from different CHRs (i.e. autosomes as well as sex chromosomes) and variants from multiple population individuals together??
Thank you very much for your kind reply in advance!