Simulate a single data set consisting of n subjects and 2 phenotypes for each

sim1(X, B, Vg, Ve, kinship)

Arguments

X

design matrix (incorporating genotype probabilities from two loci), 2n by 2f

B

a matrix of allele effects, f rows by 2 columns

Vg

a genetic covariance matrix, 2 by 2

Ve

an error covariance matrix, 2 by 2

kinship

a chromosome-specific kinship matrix, n by n