Hello,
I'm working with RAD-seq data in Stacks. And I obtained my final dataset in .PED format. Then I converted the plink PED file (.ped and .map) into a .BED format file using the following command:
plink -file input.plink --set-missing-var-ids "@_#" --make-bed --out output.file --allow-extra-chr --mind 0.3 --geno 0
And I was wondering how I should interpret the coding of the alleles: 0, 1 , 2. Given that I did not specify any '--recode' command I'm not sure what would be the correct interpretation:
Is it correct to interpret as:
0 homozygous for the major allele 1 heterozygous 2 homozygous for minor alleles