Missing data per marker and per individual, genotype counts, and the chi-square test of each marker against its expected Mendelian ratio (1:2:1, 3:1, 1:1). The significance threshold is Bonferroni-corrected for the number of markers.
Missing data per marker and per individual, genotype counts, and the chi-square test of each marker against its expected Mendelian ratio (1:2:1, 3:1, 1:1). The significance threshold is Bonferroni-corrected for the number of markers.