####=========================================####
#### For CRAN time limitations most lines in the
#### examples are silenced with one '#' mark,
#### remove them and run the examples
####=========================================####
data(CPdata)
CPpheno <- CPdata$pheno
CPgeno <- CPdata$geno
### look at the data
head(CPpheno)
CPgeno[1:5,1:5]
## fit a model including additive and dominance effects
y <- CPpheno$color
Za <- diag(length(y))
Zd <- diag(length(y))
Ze <- diag(length(y))
A <- A.mat(CPgeno) # additive relationship matrix
D <- D.mat(CPgeno) # dominant relationship matrix
E <- E.mat(CPgeno) # epistatic relationship matrix
y.trn <- y # for prediction accuracy
ww <- sample(c(1:dim(Za)[1]),72) # delete data for 1/5 of the population
y.trn[ww] <- NA
####================####
#### ADDITIVE MODEL ####
####================####
ETA.A <- list(list(Z=Za,K=A))
#ans.A <- mmer(y=y.trn, Z=ETA.A)
#cor(ans.A$fitted.y[ww], y[ww], use="pairwise.complete.obs")
####=========================####
#### ADDITIVE-DOMINANCE MODEL ####
####=========================####
ETA.AD <- list(list(Z=Za,K=A),list(Z=Zd,K=D))
#ans.AD <- mmer(y=y.trn, Z=ETA.AD)
#cor(ans.AD$fitted.y[ww], y[ww], use="pairwise.complete.obs")
### greater accuracy !!!! 4 percent increment!!
### we run 100 iterations, 4 percent increment in general
####===================================####
#### ADDITIVE-DOMINANCE-EPISTASIS MODEL ####
####===================================####
ETA.ADE <- list(list(Z=Za,K=A),list(Z=Zd,K=D),list(Z=Ze,K=E))
#ans.ADE <- mmer(y=y.trn, Z=ETA.ADE)
#cor(ans.ADE$fitted.y[ww], y[ww], use="pairwise.complete.obs")
#summary(ans.A)
#summary(ans.AD)
#summary(ans.ADE)
#### adding more effects doesn't necessarily increase prediction accuracy!
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