# NOT RUN {
library(DIME)
# generate simulated datasets with underlying exponential-normal components
N1 <- 1500; N2 <- 500; K <- 4; rmu <- c(-2.25,1.50); rsigma <- c(1,1);
rpi <- c(.05,.45,.45,.05); rbeta <- c(12,10);
set.seed(1234)
chr1 <- c(-rgamma(ceiling(rpi[1]*N1),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N1),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N1),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N1),shape = 1,scale = rbeta[2]));
chr2 <- c(-rgamma(ceiling(rpi[1]*N2),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N2),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N2),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N2),shape = 1,scale = rbeta[2]));
chr3 <- c(-rgamma(ceiling(rpi[1]*N2),shape = 1,scale = rbeta[1]),
rnorm(ceiling(rpi[2]*N2),rmu[1],rsigma[1]),
rnorm(ceiling(rpi[3]*N2),rmu[2],rsigma[2]),
rgamma(ceiling(rpi[4]*N2),shape = 1,scale = rbeta[2]));
# analyzing only chromosome 1 and chromosome 3
data <- list(chr1,chr3);
# run DIME with small maximum iteration and repetitions
set.seed(1234);
test <- DIME(data,gng.max.iter=10,gng.rep=1,inudge.max.iter=10,inudge.rep=1,
nudge.max.iter=10,nudge.rep=1)
# get classification based on inudge
test$inudge <- DIME.classify(data,test$inudge,obj.cutoff=0.1);
# vector of classification. 1 represents differential, 0 denotes non-differential
inudgeClass <- test$inudge$class;
# }
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