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Exam Number : A00-240
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This exam is administered by SAS and Pearson VUE.
60 scored multiple-choice and short-answer questions.
(Must achieve score of 68 percent correct to pass)
In addition to the 60 scored items, there may be up to five unscored items.
Two hours to complete exam.
Use exam ID A00-240; required when registering with Pearson VUE.

ANOVA - 10%
Verify the assumptions of ANOVA
Analyze differences between population means using the GLM and TTEST procedures
Perform ANOVA post hoc test to evaluate treatment effect
Detect and analyze interactions between factors

Linear Regression - 20%
Fit a multiple linear regression model using the REG and GLM procedures
Analyze the output of the REG, PLM, and GLM procedures for multiple linear regression models
Use the REG or GLMSELECT procedure to perform model selection
Assess the validity of a given regression model through the use of diagnostic and residual analysis

Logistic Regression - 25%
Perform logistic regression with the LOGISTIC procedure
Optimize model performance through input selection
Interpret the output of the LOGISTIC procedure
Score new data sets using the LOGISTIC and PLM procedures

Prepare Inputs for Predictive Model Performance - 20%
Identify the potential challenges when preparing input data for a model
Use the DATA step to manipulate data with loops, arrays, conditional statements and functions
Improve the predictive power of categorical inputs
Screen variables for irrelevance and non-linear association using the CORR procedure
Screen variables for non-linearity using empirical logit plots

Measure Model Performance - 25%
Apply the principles of honest assessment to model performance measurement
Assess classifier performance using the confusion matrix
Model selection and validation using training and validation data
Create and interpret graphs (ROC, lift, and gains charts) for model comparison and selection
Establish effective decision cut-off values for scoring

Verify the assumptions of ANOVA
=> Explain the central limit theorem and when it must be applied
=> Examine the distribution of continuous variables (histogram, box -whisker, Q-Q plots)
=> Describe the effect of skewness on the normal distribution
=> Define H0, H1, Type I/II error, statistical power, p-value
=> Describe the effect of demo size on p-value and power
=> Interpret the results of hypothesis testing
=> Interpret histograms and normal probability charts
=> Draw conclusions about your data from histogram, box-whisker, and Q-Q plots
=> Identify the kinds of problems may be present in the data: (biased sample, outliers, extreme values)
=> For a given experiment, verify that the observations are independent
=> For a given experiment, verify the errors are normally distributed
=> Use the UNIVARIATE procedure to examine residuals
=> For a given experiment, verify all groups have equal response variance
=> Use the HOVTEST option of MEANS statement in PROC GLM to asses response variance

Analyze differences between population means using the GLM and TTEST procedures
=> Use the GLM Procedure to perform ANOVA
o CLASS statement
o MODEL statement
o MEANS statement
o OUTPUT statement
=> Evaluate the null hypothesis using the output of the GLM procedure
=> Interpret the statistical output of the GLM procedure (variance derived from MSE, Fvalue, p-value R**2, Levene's test)
=> Interpret the graphical output of the GLM procedure
=> Use the TTEST Procedure to compare means Perform ANOVA post hoc test to evaluate treatment effect

Use the LSMEANS statement in the GLM or PLM procedure to perform pairwise comparisons
=> Use PDIFF option of LSMEANS statement
=> Use ADJUST option of the LSMEANS statement (TUKEY and DUNNETT)
=> Interpret diffograms to evaluate pairwise comparisons
=> Interpret control plots to evaluate pairwise comparisons
=> Compare/Contrast use of pairwise T-Tests, Tukey and Dunnett comparison methods Detect and analyze interactions between factors
=> Use the GLM procedure to produce reports that will help determine the significance of the interaction between factors. MODEL statement
=> LSMEANS with SLICE=option (Also using PROC PLM)
=> ODS SELECT
=> Interpret the output of the GLM procedure to identify interaction between factors:
=> p-value
=> F Value
=> R Squared
=> TYPE I SS
=> TYPE III SS

Linear Regression - 20%

Fit a multiple linear regression model using the REG and GLM procedures
=> Use the REG procedure to fit a multiple linear regression model
=> Use the GLM procedure to fit a multiple linear regression model

Analyze the output of the REG, PLM, and GLM procedures for multiple linear regression models
=> Interpret REG or GLM procedure output for a multiple linear regression model:
=> convert models to algebraic expressions
=> Convert models to algebraic expressions
=> Identify missing degrees of freedom
=> Identify variance due to model/error, and total variance
=> Calculate a missing F value
=> Identify variable with largest impact to model
=> For output from two models, identify which model is better
=> Identify how much of the variation in the dependent variable is explained by the model
=> Conclusions that can be drawn from REG, GLM, or PLM output: (about H0, model quality, graphics)
Use the REG or GLMSELECT procedure to perform model selection

Use the SELECTION option of the model statement in the GLMSELECT procedure
=> Compare the differentmodel selection methods (STEPWISE, FORWARD, BACKWARD)
=> Enable ODS graphics to display graphs from the REG or GLMSELECT procedure
=> Identify best models by examining the graphical output (fit criterion from the REG or GLMSELECT procedure)
=> Assign names to models in the REG procedure (multiple model statements)
Assess the validity of a given regression model through the use of diagnostic and residual analysis
=> Explain the assumptions for linear regression
=> From a set of residuals plots, asses which assumption about the error terms has been violated
=> Use REG procedure MODEL statement options to identify influential observations (Student Residuals, Cook's D, DFFITS, DFBETAS)
=> Explain options for handling influential observations
=> Identify collinearity problems by examining REG procedure output
=> Use MODEL statement options to diagnose collinearity problems (VIF, COLLIN, COLLINOINT)

Logistic Regression - 25%
Perform logistic regression with the LOGISTIC procedure
=> Identify experiments that require analysis via logistic regression
=> Identify logistic regression assumptions
=> logistic regression concepts (log odds, logit transformation, sigmoidal relationship between p and X)
=> Use the LOGISTIC procedure to fit a binary logistic regression model (MODEL and CLASS statements)

Optimize model performance through input selection
=> Use the LOGISTIC procedure to fit a multiple logistic regression model
=> LOGISTIC procedure SELECTION=SCORE option
=> Perform Model Selection (STEPWISE, FORWARD, BACKWARD) within the LOGISTIC procedure

Interpret the output of the LOGISTIC procedure
=> Interpret the output from the LOGISTIC procedure for binary logistic regression models: Model Convergence section
=> Testing Global Null Hypothesis table
=> Type 3 Analysis of Effects table
=> Analysis of Maximum Likelihood Estimates table

Association of Predicted Probabilities and Observed Responses
Score new data sets using the LOGISTIC and PLM procedures
=> Use the SCORE statement in the PLM procedure to score new cases
=> Use the CODE statement in PROC LOGISTIC to score new data
=> Describe when you would use the SCORE statement vs the CODE statement in PROC LOGISTIC
=> Use the INMODEL/OUTMODEL options in PROC LOGISTIC
=> Explain how to score new data when you have developed a model from a biased sample
Prepare Inputs for Predictive Model

Performance - 20%
Identify the potential challenges when preparing input data for a model
=> Identify problems that missing values can cause in creating predictive models and scoring new data sets
=> Identify limitations of Complete Case Analysis
=> Explain problems caused by categorical variables with numerous levels
=> Discuss the problem of redundant variables
=> Discuss the problem of irrelevant and redundant variables
=> Discuss the non-linearities and the problems they create in predictive models
=> Discuss outliers and the problems they create in predictive models
=> Describe quasi-complete separation
=> Discuss the effect of interactions
=> Determine when it is necessary to oversample data

Use the DATA step to manipulate data with loops, arrays, conditional statements and functions
=> Use ARRAYs to create missing indicators
=> Use ARRAYS, LOOP, IF, and explicit OUTPUT statements

Improve the predictive power of categorical inputs
=> Reduce the number of levels of a categorical variable
=> Explain thresholding
=> Explain Greenacre's method
=> Cluster the levels of a categorical variable via Greenacre's method using the CLUSTER procedure
o METHOD=WARD option
o FREQ, VAR, ID statement

Use of ODS output to create an output data set
=> Convert categorical variables to continuous using smooth weight of evidence

Screen variables for irrelevance and non-linear association using the CORR procedure
=> Explain how Hoeffding's D and Spearman statistics can be used to find irrelevant variables and non-linear associations
=> Produce Spearman and Hoeffding's D statistic using the CORR procedure (VAR, WITH statement)
=> Interpret a scatter plot of Hoeffding's D and Spearman statistic to identify irrelevant variables and non-linear associations Screen variables for non-linearity using empirical logit plots
=> Use the RANK procedure to bin continuous input variables (GROUPS=, OUT= option; VAR, RANK statements)
=> Interpret RANK procedure output
=> Use the MEANS procedure to calculate the sum and means for the target cases and total events (NWAY option; CLASS, VAR, OUTPUT statements)
=> Create empirical logit plots with the SGPLOT procedure
=> Interpret empirical logit plots

Measure Model Performance - 25%
Apply the principles of honest assessment to model performance measurement
=> Explain techniques to honestly assess classifier performance
=> Explain overfitting
=> Explain differences between validation and test data
=> Identify the impact of performing data preparation before data is split Assess classifier performance using the confusion matrix
=> Explain the confusion matrix
=> Define: Accuracy, Error Rate, Sensitivity, Specificity, PV+, PV-
=> Explain the effect of oversampling on the confusion matrix
=> Adjust the confusion matrix for oversampling

Model selection and validation using training and validation data
=> Divide data into training and validation data sets using the SURVEYSELECT procedure
=> Discuss the subset selection methods available in PROC LOGISTIC
=> Discuss methods to determine interactions (forward selection, with bar and @ notation)

Create interaction plot with the results from PROC LOGISTIC
=> Select the model with fit statistics (BIC, AIC, KS, Brier score)
Create and interpret graphs (ROC, lift, and gains charts) for model comparison and selection
=> Explain and interpret charts (ROC, Lift, Gains)
=> Create a ROC curve (OUTROC option of the SCORE statement in the LOGISTIC procedure)
=> Use the ROC and ROCCONTRAST statements to create an overlay plot of ROC curves for two or more models
=> Explain the concept of depth as it relates to the gains chart

Establish effective decision cut-off values for scoring
=> Illustrate a decision rule that maximizes the expected profit
=> Explain the profit matrix and how to use it to estimate the profit per scored customer
=> Calculate decision cutoffs using Bayes rule, given a profit matrix
=> Determine optimum cutoff values from profit plots
=> Given a profit matrix, and model results, determine the model with the highest average profit



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Jessica Leung, MPH*, Adriana S. Lopez, MHS*, Joel Blostein, MPH†, Nancy Thayer, RN‡, Jennifer Zipprich, PhD§, Anna Clayton, MPH§, Vicki Buttery, MS¶, Jannifer Andersen, RN||, Carrie A. Thomas, PhD**, Maria del Rosario, MD, MPH**, Kurt Seetoo, MPH††, Tracy Woodall, DVM, MPH‡‡, Rachel Wiseman, MPH§§ and Stephanie R. Bialek, MD, MPH*

*Division of Viral ailments, country wide center for Immunization and Respiratory diseases, centers for ailment control and Prevention, Atlanta, Georgia; †Division of Immunization, Michigan branch of neighborhood health, Lansing, Michigan; ‡Vermont branch of health, Burlington, Vermont; §Immunization department, California department of Public fitness, Richmond, California; ¶Vaccine-Preventable ailment Unit, Minnesota branch of fitness, St. Paul, Minnesota; ||office of Epidemiology, Mississippi State department of fitness, Jackson, Mississippi; **West Virginia department of health and Human elements, Charleston, West Virginia; ††Infectious ailment Epidemiology and Outbreak Response Bureau, center for Immunization, Maryland branch of fitness and intellectual Hygiene, Baltimore, Maryland; ‡‡disorder control and Environmental Epidemiology Division, Colorado department of Public fitness and ambiance, Denver, Colorado; and §§Infectious disorder manage Unit, Texas department of State fitness services, Austin, Texas.

address for correspondenceJessica Leung, MPH, facilities for ailment handle and Prevention, 1600 Clifton Rd NE, MS A-34, Atlanta, GA 30333. e mail: JLeung@cdc.gov.




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