PROG8430 – Data Analysis, Modeling and Algorithms Assignment 5 Classification DUE BEFORE 10PM APRIL 25, 2021 1. Submission Guidelines All assignments must be submitted via the econestoga course...

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PROG8430 – Data Analysis, Modeling and Algorithms Assignment 5 Classification DUE BEFORE 10PM APRIL 25, 2021 1. Submission Guidelines All assignments must be submitted via the econestoga course website before the due date in to the assignment folder. You may make multiple submissions, but only the most current submission will be graded. SUBMISSIONS In the Assignment 5 Folder submit: 1. Your R Code 2. Your report in Word PLEASE DO NOT SUBMIT ZIPPED FILES All variables in your code must abide by the naming convention [variable_name]_[intials]. For example, a variable I create for State would be State_DM. You may only use the ‘R’ packages discussed and demonstrated in class: 1. pROC 2. MASS 3. klaR THIS IS AN INDIVIDUAL ASSIGNMENT. UNAUTHORIZED COLLABORATION IS AN ACADEMIC OFFENSE. Please see the Conestoga College Academic Integrity Policy for details. 2. Grading This assignment will be marked out of 30 and is worth 15% of your total grade in the course. Late assignments will receive a 20% penalty. Assignments received after start of class the day after due will receive a mark of 0. 3. Data Each student will be using one dataset: Tumor21W.csv 4. Background The dataset contains medical information used in the pre-screening diagnosis of tumors. Your task is to use logistic regression to determine the factors that predict probability of a tumor diagnosis. You will then be using two other classification techniques and will compare all three of them. Your work should follow the format of the sample report used previously. 5. Assignment Tasks Nbr Description Marks 1 Data Transformation 1. As demonstrated in class, change your variables to workable names and transform any variables that are required to conduct the analysis. 1 2 Exploratory Analysis 1. Correlations: Create numeric correlations (as demonstrated) and comment on what you see. Are there co-linear variables? 2. Identify the two most significant predictors of tumors and provide statistical evidence (in addition to the correlation coefficients) that suggest they are associated with tumors (Think of the contingency tables we did in class). 1 2 3 Model Development As demonstrated in class, create three models. 1. A forward selection model. 2. Two additional models using variables that you select based on the above output (recall lecture slides on variable selection). We will refer to these models as “User Model 1” and “User Model 2”. Make sure you mention why you chose the variables you did. For each model, interpret and comment on the main measures we discussed in class: 1. Fisher’s Scoring Iteration (does it converge?) 2. AIC 3. Deviance 4. Residual symmetry 5. z-values 6. Variable Co-Efficients 1 2 4 Model Evaluation 1. For User Model 1 and User Model 2, create and evaluate the confusion matrix. Set the default predictive level to 50% for “success”. Based on the confusion matrix, calculate and comment on: a. Accuracy b. Specificity c. Sensitivity d. Precision 2 2. For each of the two models, create the ROC curve and calculate the AUC. Comment on how you interpret each of them. 2 5 Final Recommendation 1. Based on your preceding analysis, recommend which model should be selected and explain why. 1 SECOND PART 1 Logistic Regression – Stepwise 1. As above, use the forward option in the glm function to fit the model 2. Summarize the results in a Confusion Matrix . 3. As demonstrated in class, calculate the time (in seconds) it took to fit the model and include this in your summary. 1 1 1 2 Naïve-Bayes Classification 1. As demonstrated in class, transform the variables as necessary for N-B classification. 2. Use all the variables in the dataset to fit a Naïve-Bayesian classification model. 3. Summarize the results in a Confusion Matrix. 4. As demonstrated in class, calculate the time (in seconds) it took to fit the model and include this in your summary. 1 1 1 1 3 Linear Discriminant Analysis 1. As demonstrated in class, transform the variables as necessary for LDA classification. 2. Use all the variables in the dataset to fit an LDA classification model. 3. Summarize the results in a Confusion Matrix. 4. As demonstrated in class, calculate the time (in seconds) it took to fit the model and include this in your summary. 1 1 1 1 4 Compare All Three Classifiers For all questions below please provide evidence. 1. Which classifier is most accurate? (provide evidence) 2. Which classifier is most suitable when processing speed is most important? 3. Which classifier minimizes Type 1 errors? 4. Which classifier minimizes Type 2 errors? 5. Which classifier is best overall? 6. How do these classifiers compare to the best model you built in Part 1? 4 5 Professionalism and Clarity 3 APPENDIX ONE: DATA DICTIONARY Name Description Out Tumor is present=2, Is not present=1 Age Older =2, Younger=1 Sex Male=2, Female=1 Bone Bone Density Test: Good=1, Bad=2 Marrow Bone Marrow: Good=1, Bad=2 Lung Spot on Lung: Yes=2, No=1 Pleura Pleura: Yes=2, No=1 Liver Spot on Liver: Yes=2, No=1 Brain Brain Scan: Yes=2, No=1 Skin Lesions: Yes=2, No=1 Neck Stiff Neck? Yes=2, No=1 Supra Supraclavicular: Yes=1, No=2 Axil Axillar: Yes=1, No=2 Media Mediastinum: Yes=2, No=1
Answered 1 days AfterApr 13, 2021

Answer To: PROG8430 – Data Analysis, Modeling and Algorithms Assignment 5 Classification DUE BEFORE 10PM APRIL...

Naveen answered on Apr 15 2021
147 Votes
# Installing required packages
install.packages('dplyr')
install.packages('pROC')
install.packages('MASS')
install.packages('klaR')
# Calling libraries
library(dplyr)
library(pROC)
library(MASS)
library(klaR)
#
Reading data to R
Tumor <- read.csv('tumor21w-ky4vufl1-got3omwl.csv')
# Checking the data
head(Tumor)
# Structure of the data
str(Tumor)
# 1.1
# Changing the column names as interpretable
names(Tumor) <- c('Output','Age','Gender','Bone','Marrow','Lung','Pleura',
'Liver','Brain','Skin','Neck','Supra','Axil','Media')
# Changing the data types of variables
Tumor$Output <- Tumor$Output-1
Tumor$Age <- Tumor$Age-2
Tumor$Gender <- Tumor$Gender-1
Tumor$Bone <- Tumor$Bone-1
Tumor$Marrow <- Tumor$Marrow-1
Tumor$Lung <- Tumor$Lung-1
Tumor$Pleura <- Tumor$Pleura-1
Tumor$Liver <- Tumor$Liver-1
Tumor$Brain <- Tumor$Brain-1
Tumor$Skin <- Tumor$Skin-1
Tumor$Neck <- Tumor$Neck-1
Tumor$Supra <- Tumor$Supra-1
Tumor$Axil <- Tumor$Axil-1
Tumor$Media <- Tumor$Media-1
# 2.1
# Correlation matrix
cor(Tumor, method = "spearman")
#2.2
# Knowing the best predictors using contingency analysis
chisq.test(Tumor$Output,Tumor$Age)
chisq.test(Tumor$Output,Tumor$Gender)
chisq.test(Tumor$Output,Tumor$Bone)
chisq.test(Tumor$Output,Tumor$Marrow)
chisq.test(Tumor$Output,Tumor$Lung)
chisq.test(Tumor$Output,Tumor$Pleura)
chisq.test(Tumor$Output,Tumor$Liver)
chisq.test(Tumor$Output,Tumor$Brain)
chisq.test(Tumor$Output,Tumor$Skin)
chisq.test(Tumor$Output,Tumor$Neck)
chisq.test(Tumor$Output,Tumor$Supra)
chisq.test(Tumor$Output,Tumor$Axil)
chisq.test(Tumor$Output,Tumor$Media)
#3.1
# Forward regression model
Logit_model <- glm(formula=Output~.,data=Tumor,family = 'binomial',na.action = na.omit)
step(Logit_model,direction = 'forward')
#3.2
# Model1
Model1 <- glm(formula = Output~Gender+Bone+Skin,data=Tumor,family = 'binomial')
summary(Model1)
# Model2
Model2 <- glm(formula = Output~Neck+Media+Axil, data=Tumor)
summary(Model2)
# 4.1
# Making prediction on model1 and confusion matrix
# Predicting for the model1
pred1 <- predict(Model1, type="response")
# Converting probabilities as values
Class_pre <- ifelse(pred1 >...
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