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target_predictions.R
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target_predictions.R
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# Title : Women in data Science Datathon 2021
# Objective : Classification Problem, predict diabetes yes/no
# Team : SuperSweet
# Related rscripts: data_processing.R, target_prediction.R, functions.R
# Created on: 2/18/2021, by Manuela Runge
###----------------------------------------
###----------------------------
### SETTINGS
###----------------------------
### Load packages
library(tidyverse) # data handling using pipes
library(data.table) # faster reading of csv files
library(caret) # machin learning package
library(caTools) # confusion matrix table
library(ranger) # faster implementation of randomForest
### Custom settings
source(file.path("functions.R"))
# Define directories
getwd()
data_dir <- list.files(getwd(), "download_dat")
list.files(data_dir)
###------------------------------------------------
### Load data
###------------------------------------------------
train_df <- fread(file.path(data_dir, "TrainingWiDS2021_cleaned.csv"))
train_df$diabetes_mellitus <- factor(train_df$diabetes_mellitus,
levels=c('nodiabetes','diabetes'),
labels=c('nodiabetes','diabetes'))
table(train_df$diabetes_mellitus)
### Codebook
codebook <- fread(file.path(data_dir, "DataDictionaryWiDS2021.csv"))
colnames(codebook) <- gsub(" ", "_", tolower(colnames(codebook)))
cols_not_exist <- which(!((unique(codebook$variable_name)) %in% (colnames(train_df))))
(vars_not_exist <- unique(codebook$variable_name)[cols_not_exist])
codebook <- codebook %>% filter(variable_name != vars_not_exist)
cols_cat <- f_cols_by_cat()
demographic <- c("age","bmi","gender","ethnicity")
comorbidity <- cols_cat$apachecomorbidity
###------------------------------------------------
### Different options for pre-selecting features
###------------------------------------------------
cols_highvariance <- fread(file.path(data_dir,"cols_highvariance.csv"))
cols_highvariance <- cols_highvariance$cols_highvariance
cols_highassociation <- c("age", "bmi", "height", "weight","glucose_apache", "d1_glucose_max",
"h1_glucose_max","d1_glucose_min", "h1_glucose_min", "d1_creatinine_min",
"d1_creatinine_max")
selected_features_A <- c("d1_glucose_max")
selected_features_B <- c(demographic, comorbidity)
selected_features_C <- cols_highvariance
selected_features_D <- c(selected_features_B, cols_highvariance)
selected_features_E <- c(cols_highvariance,cols_highassociation)
selected_features_F = cols_highassociation
### Select features --------------------------
selected_predictors <- selected_features_F ### Feature selection
selected_predictors <- unique(selected_predictors)
train_df <- as.data.frame(train_df)
train_df <- train_df[,(colnames(train_df) %in% c( "diabetes_mellitus",selected_predictors))]
dim(train_df)
###------------------------------------------------
### CARET preprocessing
###------------------------------------------------
### Select preprocessing steps and create preprocessing object to apply on train and test data
#c("zv", "medianImpute","center", "scale","pca") #c("zv", "medianImpute","center", "scale" , "pca") #"corr"
preprocessing=c("medianImpute")
preProc <- preProcess(train_df, method =preprocessing)
train_df_prep <- predict(preProc,train_df )
dim(train_df_prep)
### Split dataframe for easier processing in caret train function
diabetes_mellitus_x <- train_df_prep %>% select(-diabetes_mellitus)
diabetes_mellitus_y <- train_df_prep %>% select(diabetes_mellitus)
diabetes_mellitus_y <- diabetes_mellitus_y$diabetes_mellitus
###----------------------------
### CARET settings
###----------------------------
### Get information about available methods
names(getModelInfo())
### Get information about preprocessing options
?preProcess
# Create custom indices: myFolds
myFolds <- createFolds(diabetes_mellitus_y, k = 5)
# Create reusable trainControl object: myControl
myControl <- trainControl(
summaryFunction = twoClassSummary,
classProbs = TRUE, # IMPORTANT!
verboseIter = TRUE,
savePredictions = TRUE,
index = myFolds
)
###----------------------------
### TRAIN MODELS
### Note random Forest takes very long
### --------------------
TEST=FALSE
methods = c("glm","ranger","glmnet")
if(TEST)methods="glm"
model_list <- list()
for( method in methods){
#method=methods[1]
model <- train(
x = diabetes_mellitus_x,
y = diabetes_mellitus_y,
metric = "ROC",
method = method,
trControl = myControl
)
model_list[[method]] <- model
}
### Investigate specific model
temp_model <- model_list$glm
p = predict(temp_model, train_df_prep,type = "prob")
dim(p)
p_class <- ifelse(p[,2] > 0.5, "diabetes", "nodiabetes")
p_class <- factor(p_class, levels=c( "nodiabetes","diabetes"),
labels=c("nodiabetes","diabetes"))
confusionMatrix(p_class, train_df_prep$diabetes_mellitus)
colAUC(p, train_df_prep$diabetes_mellitus, plotROC = TRUE)
## Investigate caret objects
names(temp_model)
dim(diabetes_mellitus_x)
dim(temp_model$trainingData)
#### Compare models and summarize/visualize results
if(length(model_list)> 1){
resamp = resamples(model_list)
# Summarize the results
summary(resamp)
dotplot(resamp, metric="ROC")
xyplot(resamp, metric="ROC" )
}
###----------------------------
### MAKE PREDICTIONS on unlabelled data
###----------------------------
## Load and clean test data
test_df <- fread(file.path(data_dir, "UnlabeledWiDS2021.csv")) %>%
as.data.frame() %>%
arrange(encounter_id) %>%
select(selected_predictors)
dim(test_df)
### Apply same preprocessing as for train data!
str(test_df)
test_dat_prep <- predict(preProc, test_df)
str(test_dat_prep)
## Make predictions and save csv
submit_df <- f_predict_and_save_submission_csv(test_dat=test_dat_prep,
model_list=model_list,
final_method="glm")
### Look at predictions
summary(submit_df$diabetes_mellitus)
p_class_test <- ifelse(submit_df$diabetes_mellitus > 0.5, "diabetes", "nodiabetes")
table(p_class_test)
(length(p_class_test[p_class_test=="diabetes"] )/ length(p_class_test))*100