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Lecture 13 Diagnostics in MLR Variance Inflation Factors Added variable plots Identifying outliers BMTRY 701 Biostatistical Methods II

BMTRY 701 Biostatistical Methods II

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Lecture 13 Diagnostics in MLR Variance Inflation Factors Added variable plots Identifying outliers. BMTRY 701 Biostatistical Methods II. Variance Inflation Factor (VIF). Diagnostic for multicollinearity Describes the amount of an X that is explained by the other X’s in the model - PowerPoint PPT Presentation

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Page 1: BMTRY 701 Biostatistical Methods II

Lecture 13

Diagnostics in MLRVariance Inflation FactorsAdded variable plotsIdentifying outliers

BMTRY 701Biostatistical Methods II

Page 2: BMTRY 701 Biostatistical Methods II

Variance Inflation Factor (VIF)

Diagnostic for multicollinearity Describes the amount of an X that is explained

by the other X’s in the model If VIF is high, then it suggests that the covariate

should not be added. Why?

• it is redundant• it adds variance to the model• it creates ‘instability’ in the estimation

Page 3: BMTRY 701 Biostatistical Methods II

How to calculate VIF?

Simple idea:

That is, the VIF for the jth covariate is the coefficient of determination (R2) obtained from regressing xj on the remaining x’s in the model

21

1

jj R

VIF

exxxxx JJjjjjj 1111110

Page 4: BMTRY 701 Biostatistical Methods II

Sounds like a lot of work!

You don’t actually have to estimate the regressions for each xj.

Some matrix notation:• X = matrix of covariates including a column for the intercept• XT = transpose of X. That is, flip X on its diagonal• X-1 = the inverse of X. That is, what you multiply X by to get the

identity matrix• I = the identity matrix. A matrix with 0’s on the off-diagonal and

1’s on the diagonal

Useful matrix: XTX. (see chapter 3 for lots on it!) Another useful matrix: (XTX)-1

Page 5: BMTRY 701 Biostatistical Methods II

XTX

Recall what it means to standardize a variable:• subtract off the mean• divide by the standard deviation

Imagine that you standardize all of the variables in your model (x’s).

Call the new covariate matrix W Now, if calculate WTW (and divide by n-1), it is

the correlation matrix Lastly, take the inverse of WTW (i.e., (WTW)-1)

Page 6: BMTRY 701 Biostatistical Methods II

VIFs

The diagonals of the (WTW)-1 matrix are the VIFs This is a natural by-product of the regression The (WTW)-1 matrix is estimated when the

regression is estimated

Rules of thumb:• VIF larger than 10 implies a serious multicollinearity

problem• VIFs of 5 or greater suggest that coefficient estimates

may be misleading due to multicollinearity

Page 7: BMTRY 701 Biostatistical Methods II

Getting the VIFs the old-fashioned way

# standardize variablesages <- (AGE-mean(AGE))/sqrt(var(AGE))censuss <- (CENSUS - mean(CENSUS))/sqrt(var(CENSUS))xrays <- (XRAY - mean(XRAY))/sqrt(var(XRAY))infrisks <- (INFRISK-mean(INFRISK))/sqrt(var(INFRISK))sqrtcults <- (sqrtCULT-mean(sqrtCULT))/sqrt(var(sqrtCULT))nurses <- (NURSE - mean(NURSE))/sqrt(var(NURSE))

# create matrix of covariatesxmat <- data.frame(ages, censuss, xrays, infrisks, sqrtcults, nurses)xmat <- as.matrix(xmat)n <- nrow(xmat) # estimate x-transpose x and divide by n-1cormat <- t(xmat)%*%xmat/(n-1)

# solve finds the inverse of a matrixvifmat <- solve(cormat)

round(diag(vifmat), 2)

Page 8: BMTRY 701 Biostatistical Methods II

More practical way.

library(HH)mlr <- lm(logLOS ~ AGE + CENSUS + XRAY +

INFRISK + sqrtCULT + NURSE)

round(diag(vifmat), 2) ages censuss xrays infrisks sqrtcults nurses 1.10 5.88 1.39 2.01 1.92 5.94

vif(mlr)

AGE CENSUS XRAY INFRISK sqrtCULT NURSE 1.096204 5.875625 1.390417 2.007692 1.916983 5.935711

Page 9: BMTRY 701 Biostatistical Methods II

What to do?

Unlikely that only one variable will have high VIF You need to then determine which to include,

which to remove Judgement should be based on science +

statistics!

Page 10: BMTRY 701 Biostatistical Methods II

More diagnostics: the added variable plots

These can help check for adequacy of model Is there curvature between Y and X after

adjusting for the other X’s? “Refined” residual plots They show the marginal importance of an

individual predictor Help figure out a good form for the predictor

Page 11: BMTRY 701 Biostatistical Methods II

Example: SENIC

Recall the difficulty determining the form for INFIRSK in our regression model.

Last time, we settled on including one term, INFRISK^2

But, we could do an adjusted variable plot approach.

How? We want to know, adjusting for all else in the

model, what is the right form for INFRISK?

Page 12: BMTRY 701 Biostatistical Methods II

R code

av1 <- lm(logLOS ~ AGE + XRAY + CENSUS + factor(REGION) )av2 <- lm(INFRISK ~ AGE + XRAY + CENSUS + factor(REGION) )resy <- av1$residualsresx <- av2$residuals

plot(resx, resy, pch=16)

abline(lm(resy~resx), lwd=2)

Page 13: BMTRY 701 Biostatistical Methods II

Added Variable Plot

-2 -1 0 1 2 3

-0.2

0.0

0.2

0.4

resx

resy

Page 14: BMTRY 701 Biostatistical Methods II

What does that show?

The relationship between logLOS and INFRISK if you added INFRISK to the regression

But, is that what we want to see? How about looking at residuals versus INFRISK

(before including INFRISK in the model)?

Page 15: BMTRY 701 Biostatistical Methods II

R codemlr8 <- lm(logLOS ~ AGE + XRAY + CENSUS + factor(REGION))smoother <- lowess(INFRISK, mlr8$residuals)plot(INFRISK, mlr8$residuals)lines(smoother)

2 3 4 5 6 7 8

-0.2

0.0

0.2

0.4

INFRISK

mlr

8$

resi

du

als

Page 16: BMTRY 701 Biostatistical Methods II

R code

> infrisk.star <- ifelse(INFRISK>4,INFRISK-4,0)> mlr9 <- lm(logLOS ~ INFRISK + infrisk.star + AGE + XRAY + > CENSUS + factor(REGION))> summary(mlr9)

Coefficients: Estimate Std. Error t value Pr(>|t|) (Intercept) 1.798e+00 1.667e-01 10.790 < 2e-16 ***INFRISK 1.836e-03 1.984e-02 0.093 0.926478 infrisk.star 6.795e-02 2.810e-02 2.418 0.017360 * AGE 5.554e-03 2.535e-03 2.191 0.030708 * XRAY 1.361e-03 6.562e-04 2.073 0.040604 * CENSUS 3.718e-04 7.913e-05 4.698 8.07e-06 ***factor(REGION)2 -7.182e-02 3.051e-02 -2.354 0.020452 * factor(REGION)3 -1.030e-01 3.036e-02 -3.391 0.000984 ***factor(REGION)4 -2.068e-01 3.784e-02 -5.465 3.19e-07 ***---Signif. codes: 0 ‘***’ 0.001 ‘**’ 0.01 ‘*’ 0.05 ‘.’ 0.1 ‘ ’ 1

Residual standard error: 0.1137 on 104 degrees of freedomMultiple R-Squared: 0.6209, Adjusted R-squared: 0.5917 F-statistic: 21.29 on 8 and 104 DF, p-value: < 2.2e-16

Page 17: BMTRY 701 Biostatistical Methods II

Residual Plots

2 3 4 5 6 7 8

-0.2

-0.1

0.0

0.1

0.2

0.3

0.4

INFRISK

mlr

9$

resi

du

als

2 3 4 5 6 7 8

-0.2

-0.1

0.0

0.1

0.2

0.3

0.4

INFRISK

mlr

7$

resi

du

als

SPLINE FOR INFRISK INFRISK2

Page 18: BMTRY 701 Biostatistical Methods II

Which is better?

Cannot compare via ANOVA because they are not nested!

But, we can compare statistics qualitatively R-squared:

• MLR7: 0.60• MLR9: 0.62

Partial R-squared:• MLR7: 0.17• MLR9: 0.19

Page 19: BMTRY 701 Biostatistical Methods II

Identifying Outliers

Harder to do in the MLR setting than in the SLR setting.

Recall two concepts that make outliers important: • Leverage is a function of the explanatory variable(s)

alone and measures the potential for a data point to affect the model parameter estimates.

• Influence is a measure of how much a data point actually does affect the estimated model.

Leverage and influence both may be defined in terms of matrices

Page 20: BMTRY 701 Biostatistical Methods II

“Hat” matrix

We must do some matrix stuff to understand this Notation for a MLR with p predictors and data on

n patients. The data:

nY

Y

Y

Y2

1

~

npn

p

p

XX

XX

XX

X

1

221

111

1

1

1

~

Page 21: BMTRY 701 Biostatistical Methods II

More notation:

THE MODEL:

What are the dimensions of each?

Matrix Format for the MLR model

ne

e

e

e2

1

p

1

0

eXY

Page 22: BMTRY 701 Biostatistical Methods II

“Transpose” and “Inverse”

X-transpose: X’ or XT

X-inverse: X-1

Hat matrix = H

Why is H important? It transforms Y’s to Yhat’s:

')'( 1 XXXXH

HYY ˆ

Page 23: BMTRY 701 Biostatistical Methods II

Estimating, based on fitted model

)()(2 HIMSEes

Variance-Covariance Matrix of residuals:

)1()(2iii hMSEes

Variance of ith residual:

MSEhhses ijijij )0()( 22

Covariance of ith and jth residual:

Page 24: BMTRY 701 Biostatistical Methods II

Other uses of H

YHIe )(

I = identity matrix

)()( 22 HIe

Variance-Covariance Matrix of residuals:

)1()( 22iii he

Variance of ith residual:

222 )0()( ijijij hhe

Covariance of ith and jth residual:

Page 25: BMTRY 701 Biostatistical Methods II

Property of hij’s

n

i

n

jijij hh

1 1

1

This means that each row of H sums to 1And, that each column of H sums to 1

Page 26: BMTRY 701 Biostatistical Methods II

Other use of H

Identifies points of leverage

0 5 10 15

-10

01

02

03

04

0

x

y

1 2

4

3

Page 27: BMTRY 701 Biostatistical Methods II

Using the Hat Matrix to identify outliers

Look at hii to see if a datapoint is an outlier Large values of hii imply small values of var(ei) As hii gets close to 1, var(ei) approaches 0. Note that

As hii approaches 1, yhat approaches y This gives hii the name “leverage” HIGH HAT VALUE IMPLIES POTENTIAL FOR

OUTLIER!

ji

jijiii

n

jjiji yhyhyhy

1

ˆ

Page 28: BMTRY 701 Biostatistical Methods II

R code

hat <- hatvalues(reg)plot(1:102, hat)highhat <- ifelse(hat>0.10,1,0)plot(x,y)points(x[highhat==1], y[highhat==1],

col=2, pch=16, cex=1.5)

Page 29: BMTRY 701 Biostatistical Methods II

Hat values versus index

0 20 40 60 80 100

0.0

20

.06

0.1

00

.14

1:102

ha

t

Page 30: BMTRY 701 Biostatistical Methods II

Identifying points with high hii

0 5 10 15

-10

01

02

03

04

0

x

y

Page 31: BMTRY 701 Biostatistical Methods II

Does a high hat mean it has a large residual?

No. hii measures leverage, not influence Recall what hii is made of

• it depends ONLY on the X’s• it does not depend on the actual Y value

Look back at the plot: which of these is probably most “influential”

Standard cutoffs for “large” hii: • 2p/n• 0.5 very high, 0.2-0.5 high

Page 32: BMTRY 701 Biostatistical Methods II

Let’s look at our MLR9

Any outliers?

0 20 40 60 80 100

0.0

50

.10

0.1

50

.20

1:length(hat9)

ha

t9

Page 33: BMTRY 701 Biostatistical Methods II

Using the hat matrix in MLR

Studentized residuals Acknowledge:

• each residual has a different variance• magnitude of residual should be made relative to its

variance (or sd)

Studentized residuals recognize differences in sampling errors

Page 34: BMTRY 701 Biostatistical Methods II

Defining Studentized Residuals

From slide 15,

We then define

Comparing ei and ri• ei have different variance due to sampling variations• ri have constant variance

)1()(2iii hMSEes

)1()(ii

i

i

ii

hMSE

e

es

er

Page 35: BMTRY 701 Biostatistical Methods II

Deleted Residuals

Influence is more intuitively quantified by how things change when an observation is in versus out of the estimation process

Would be more useful to have residuals in the situation when the observation is removed.

Example: • if a Yi is far out then it may be very influential in the

regression and the residual will be small• but, if that case is removed before estimating and

then the residual is calculated based on the fit, the residual would be large

Page 36: BMTRY 701 Biostatistical Methods II

Deleted Residuals, di

Process:• delete ith case• fit regression with all other cases• obtain estimate of E(Yi) based on its X’s and fitted

model

)(

)(

ˆ

estimation from removed with valuefittedˆ

iiii

iii

YYd

YY

Page 37: BMTRY 701 Biostatistical Methods II

Deleted Residuals, di

Nice result: you don’t actually have to refit without the ith case!

where ei is the ‘plain’ residual from the ith case and hii is the hat value. Both are from the regression INCLUDING the case

For small hii: ei and di will be similar For large hii: ei and di will be different

ii

ii h

ed

1

Page 38: BMTRY 701 Biostatistical Methods II

Studentized Deleted Residuals

Recall the need to standardize, based on the knowledge of the variance

The difference between ti and ri?

)1(

)(

)( iii

i

i

ii

hMSE

e

ds

dt

Page 39: BMTRY 701 Biostatistical Methods II

Another nice result

You can calculate MSE(i) without refitting the model

2/1

2)1(

1

iiiii ehSSE

pnet

Page 40: BMTRY 701 Biostatistical Methods II

Testing for outliers

outlier = Y observations whose studentized deleted residuals are large (in absolute value)

ti ~ t with n-p-1 degrees of freedom

Two examples: • simulated data• mlr9