Form principal components predictor from a trained superpc object
Computes supervised principal components, using scores from "object"
superpc.predict(object, data, newdata, threshold, n.components=3, prediction.type=c("continuous","discrete","nonzero"), n.class=2)
object |
Obect returned by superpc.train |
data |
List of training data, of form described in superpc.train documentation, |
newdata |
List of test data; same form as training data |
threshold |
Threshold for scores: features with abs(score) > threshold are retained. |
n.components |
Number of principal components to compute. Should be 1,2 or 3. |
prediction.type |
"continuous" for raw principal component(s); "discrete" for principal component categorized in equal bins; "nonzero" for indices of features that pass the threshold |
n.class |
Number of classes into which predictor is binned (for prediction.type="discrete" |
v.pred |
Supervised principal componients predictor |
u |
U matrix from svd of feature matrix x |
d |
singual values from svd of feature matrix x |
which.features |
Indices of features exceeding threshold |
n.components |
Number of supervised principal components requested |
call |
calling sequence |
"Eric Bair, Ph.D."
"Jean-Eudes Dazard, Ph.D."
"Rob Tibshirani, Ph.D."
Maintainer: "Jean-Eudes Dazard, Ph.D."
E. Bair and R. Tibshirani (2004). "Semi-supervised methods to predict patient survival from gene expression data." PLoS Biol, 2(4):e108.
E. Bair, T. Hastie, D. Paul, and R. Tibshirani (2006). "Prediction by supervised principal components." J. Am. Stat. Assoc., 101(473):119-137.
set.seed(332) #generate some data x <- matrix(rnorm(50*30), ncol=30) y <- 10 + svd(x[1:50,])$v[,1] + .1*rnorm(30) ytest <- 10 + svd(x[1:50,])$v[,1] + .1*rnorm(30) censoring.status <- sample(c(rep(1,20), rep(0,10))) censoring.status.test <- sample(c(rep(1,20), rep(0,10))) featurenames <- paste("feature", as.character(1:50), sep="") data <- list(x=x, y=y, censoring.status=censoring.status, featurenames=featurenames) data.test <- list(x=x, y=ytest, censoring.status=censoring.status.test, featurenames=featurenames) a <- superpc.train(data, type="survival") fit <- superpc.predict(a, data, data.test, threshold=1.0, n.components=1) plot(fit$v.pred, ytest)
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