# Start the graphics device driver to save all plots in a pdf format
pdf(file = "Example.pdf")
# Get the stage C prostate cancer data from the rpart package
library(rpart)
data(stagec)
# Split the stages into several columns
dataCancer <- cbind(stagec[,c(1:3,5:6)],
gleason4 = 1*(stagec[,7] == 4),
gleason5 = 1*(stagec[,7] == 5),
gleason6 = 1*(stagec[,7] == 6),
gleason7 = 1*(stagec[,7] == 7),
gleason8 = 1*(stagec[,7] == 8),
gleason910 = 1*(stagec[,7] >= 9),
eet = 1*(stagec[,4] == 2),
diploid = 1*(stagec[,8] == "diploid"),
tetraploid = 1*(stagec[,8] == "tetraploid"),
notAneuploid = 1-1*(stagec[,8] == "aneuploid"))
# Remove the incomplete cases
dataCancer <- dataCancer[complete.cases(dataCancer),]
# Load a pre-stablished data frame with the names and descriptions of all variables
data(cancerVarNames)
# Split the data set into train and test samples
trainDataCancer <- dataCancer[1:(nrow(dataCancer)/2),]
testDataCancer <- dataCancer[(nrow(dataCancer)/2+1):nrow(dataCancer),]
# Get a Cox proportional hazards model using:
# - 10 bootstrap loops
# - Train data
# - zIDI as the feature inclusion criterion
# - First order interactions
cancerModel <- ReclassificationFRESA.Model(loops = 10,
Outcome = "pgstat",
variableList = cancerVarNames,
data = trainDataCancer,
type = "COX",
timeOutcome = "pgtime",
selectionType = "zIDI",
interaction = 2)
# Predict the outcome of the test data sample
predTest <- predictForFresa(object = cancerModel$final.model,
testData = testDataCancer,
predictType = "prob")
# Shut down the graphics device driver
dev.off()
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