Nothing
getSimulatedPhenotype <-
function(data, snp.name, trait.name, covars="") {
variances <- c(1,1,1)
snp.num <- which(snpnames(data) == snp.name)
gtypes <- as.numeric(data@gtdata[ ,snp.num])
means <- getMeans(data, snp.name, trait.name)
# IMPORTANT!!! Assumes that missing have the most frequent genotype!
if (sum(is.na(gtypes)) > 0) {
warning("Missing genotypes found. Filling with the most frequent allele.")
gtypes[is.na(gtypes)] <- 0
}
freqs <- as.vector(table(gtypes)/length(gtypes))
phtypes <- rep(0, length(gtypes))
phtypes[gtypes==0] <- rnorm(length(gtypes[gtypes==0]), mean=means[1], sd=sqrt(variances[1]))
phtypes[gtypes==1] <- rnorm(length(gtypes[gtypes==1]), mean=means[2], sd=sqrt(variances[2]))
phtypes[gtypes==2] <- rnorm(length(gtypes[gtypes==2]), mean=means[3], sd=sqrt(variances[3]))
H2 <- getH2(data, snp.name, trait.name, covars)
phtypes <- phtypes + getError(H2, freqs, means, length(phtypes))
phtypes
}
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