Nothing
##' Internal cross-validation can be used for estimating the level of
##' structure in a data set and to optimise the choice of number of
##' principal components.
##'
##' This method calculates \eqn{Q^2} for a PCA model. This is the
##' cross-validated version of \eqn{R^2} and can be interpreted as the
##' ratio of variance that can be predicted independently by the PCA
##' model. Poor (low) \eqn{Q^2} indicates that the PCA model only
##' describes noise and that the model is unrelated to the true data
##' structure. The definition of \eqn{Q^2} is: \deqn{Q^2=1 -
##' \frac{\sum_{i}^{k}\sum_{j}^{n}(x -
##' \hat{x})^2}{\sum_{i}^{k}\sum_{j}^{n}x^2}}{Q^2=1 - sum_i^k sum_j^n
##' (x - \hat{x})^2 / \sum_i^k \sum_j^n(x^2)} for the matrix \eqn{x}
##' which has \eqn{n} rows and \eqn{k} columns. For a given number of
##' PC's x is estimated as \eqn{\hat{x}=TP'} (T are scores and P are
##' loadings). Although this defines the leave-one-out
##' cross-validation this is not what is performed if fold is less
##' than the number of rows and/or columns. In 'impute' type CV,
##' diagonal rows of elements in the matrix are deleted and the
##' re-estimated. In 'krzanowski' type CV, rows are sequentially left
##' out to build fold PCA models which give the loadings. Then,
##' columns are sequentially left out to build fold models for
##' scores. By combining scores and loadings from different models, we
##' can estimate completely left out values. The two types may seem
##' similar but can give very different results, krzanowski typically
##' yields more stable and reliable result for estimating data
##' structure whereas impute is better for evaluating missing value
##' imputation performance. Note that since Krzanowski CV operates on
##' a reduced matrix, it is not possible estimate Q2 for all
##' components and the result vector may therefore be shorter than
##' \code{nPcs(object)}.
##' @title Cross-validation for PCA
##' @param object A \code{pcaRes} object (result from previous PCA
##' analysis.)
##' @param originalData The matrix (or ExpressionSet) that used to
##' obtain the pcaRes object.
##' @param fold The number of groups to divide the data in.
##' @param nruncv The number of times to repeat the whole
##' cross-validation. The deletion of diagnols in 'impute' is
##' deterministic so result will alsways be the same but in
##' krzanowski where cv-split is obtained by sampling it can be
##' informative to examine the spread of the Q2 values over several
##' CV runs.
##' @param type krzanowski or imputation type cross-validation
##' @param verbose \code{boolean} If TRUE Q2 outputs a primitive
##' progress bar.
##' @param variables indices of the variables to use during
##' cross-validation calculation. Other variables are kept as they
##' are and do not contribute to the total sum-of-squares.
##' @param ... Further arguments passed to the \code{\link{pca}}
##' function called within Q2.
##' @return A matrix or vector with \eqn{Q^2} estimates.
##' @export
##' @references Krzanowski, WJ. Cross-validation in principal
##' component analysis. Biometrics. 1987(43):3,575-584
##' @examples
##' data(iris)
##' x <- iris[,1:4]
##' pcIr <- pca(x, nPcs=3)
##' q2 <- Q2(pcIr, x)
##' barplot(q2, main="Krzanowski CV", xlab="Number of PCs", ylab=expression(Q^2))
##' ## q2 for a single variable
##' Q2(pcIr, x, variables=2)
##' pcIr <- pca(x, nPcs=3, method="nipals")
##' q2 <- Q2(pcIr, x, type="impute")
##' barplot(q2, main="Imputation CV", xlab="Number of PCs", ylab=expression(Q^2))
##' @author Henning Redestig, Ondrej Mikula
##' @keywords multivariate
Q2 <- function (object, originalData=completeObs(object), fold=5,
nruncv=1, type=c("krzanowski", "impute"), verbose=interactive(),
variables=1:nVar(object), ...) {
type <- match.arg(type)
if (inherits(originalData, "ExpressionSet")) {
set <- originalData
originalData <- t(exprs(originalData))
}
if (is.null(originalData))
stop("missing data when estimating Q2")
originalData <- as.matrix(originalData)
originalData <- prep(originalData, scale=scl(object), center=center(object))
nR <- nObs(object)
nC <- nVar(object)
if (nR != nrow(originalData) | nC != ncol(originalData))
stop("data and model dimensions do not match")
if (fold > max(nR, nC))
stop("fold must be equal or less to max dimension of original data")
if (method(object) %in% c("svd") & type != "krzanowski")
stop("Chosen PCA method must use krzanowski type cv")
if (method(object) %in% c("llsImpute") & type != "impute")
stop("Chosen PCA method must use impute type cv")
if (is.logical(variables))
variables <- which(variables)
ssx <- sum(originalData[, variables]^2, na.rm=TRUE)
if(type == "impute")
nP <- nPcs(object)
if(type == "krzanowski") {
rseg <- split(sample(1:nR), rep(1:fold, ceiling(nR/fold))[1:nR])
cseg <- split(sample(1:nC), rep(1:fold, ceiling(nC/fold))[1:nC])
foldC <- length(cseg)
foldR <- length(rseg)
nP <- min(nR - max(sapply(rseg, length)),
nC - max(sapply(cseg, length)), nPcs(object))
}
q2 <- matrix(NA, nP, ncol=nruncv)
for (nr in 1:nruncv) {
press <- rep(0, nP)
if (type == "impute") {
seg <- list()
nDiag <- max(nR, nC)
diagPerFold <- floor(nDiag / fold)
suppressWarnings(diags <- matrix(1:nDiag, nrow=diagPerFold, ncol=fold, byrow=TRUE))
if (diagPerFold == 0 || diagPerFold > (nDiag/2))
stop("Matrix could not be safely divided into ",
fold, " segments. Choose a different fold or provide the desired segments")
if (nDiag%%fold > 0)
warning("Validation incomplete: ", (nDiag %% fold) * min(dim(originalData)),
" values were left out of from cross validation, Q2 estimate will be biased.")
for (i in 1:ncol(diags))
seg[[i]] <- which(is.na(deletediagonals(originalData, diags[, i])))
if (verbose) {
pb <- txtProgressBar(0, length(seg), style=3, width=20)
}
j <- 0
for (i in seg) {
j <- j + 1
if (verbose)
setTxtProgressBar(pb, j)
test <- originalData
test[i] <- NA
test <- tempFixNas(test)
if (method(object) != "llsImpute") {
pc <- pca(test, nPcs=nP, method=method(object),
verbose=FALSE, center=centered(object), scale=object@scaled, ...)
}
for (np in 1:nP) {
if (method(object) == "llsImpute") {
fittedData <- completeObs(llsImpute(test, k=np, allVariables=TRUE, center=FALSE))
}
else {
if (method(object) == "nlpca")
fittedData <- fitted(pc, data=test, nPcs=np)
else fittedData <- fitted(pc, data=NULL, nPcs=np)
}
ii <- i[ceiling(i / nR) %in% variables]
press[np] <- press[np] + sum((originalData[ii] - fittedData[ii])^2, na.rm=TRUE)
}
}
}
if (type == "krzanowski") {
rseg <- split(sample(1:nR), rep(1:fold, ceiling(nR/fold))[1:nR])
cseg <- split(sample(1:nC), rep(1:fold, ceiling(nC/fold))[1:nC])
tcv <- array(0, dim=c(foldC, nR, nP))
pcv <- array(0, dim=c(foldR, nC, nP))
for (f in 1:foldC) {
test <- tempFixNas(originalData[, -cseg[[f]]])
tcv[f, , ] <- scores(pca(test, nPcs=nP, method=method(object),
verbose=FALSE, center=centered(object), scale=object@scaled, ...))
for (p in 1:nP) {
if (cor(tcv[f, , p], scores(object)[, p]) < 0)
tcv[f, , p] <- tcv[f, , p] * -1
}
}
for (f in 1:foldR) {
test <- tempFixNas(originalData[-rseg[[f]], ])
pcv[f, , ] <- loadings(pca(test, nPcs=nP, method=method(object),
verbose=FALSE, center=centered(object), scale=object@scaled, ...))
for (p in 1:nP) {
if (cor(pcv[f, , p], loadings(object)[, p]) < 0)
pcv[f, , p] <- pcv[f, , p] * -1
}
}
press <- rep(0, nP)
for (p in 1:nP)
for (fr in 1:foldR)
for (fc in 1:foldC)
press[p] <- press[p] + sum((
originalData[rseg[[fr]], cseg[[fc]]] -
(tcv[fc, , ][, 1:p, drop=FALSE] %*% t(pcv[fr, , ][,1:p, drop=FALSE]))
[rseg[[fr]], intersect(cseg[[fc]], variables)])^2, na.rm=TRUE)
}
q2[, nr] <- 1 - press/ssx
}
if (verbose)
message("\n")
rownames(q2) <- paste("PC", 1:nrow(q2))
drop(q2)
}
##' Simply replace completely missing rows or cols with zeroes.
##' @title Temporary fix for missing values
##' @param mat a matrix
##' @return The original matrix with completely missing rows/cols
##' filled with zeroes.
##' @author Henning Redestig
tempFixNas <- function(mat) {
badRows <- apply(mat, 1, function(x) all(is.na(x)))
badCols <- apply(mat, 2, function(x) all(is.na(x)))
mat[ badRows,] <- 0
mat[,badCols ] <- 0
mat
}
##' Replace a diagonal of elements of a matrix with NA
##'
##' Used for creating artifical missing values in matrices without
##' causing any full row or column to be completely missing
##' @title Delete diagonals
##' @param x The matrix
##' @param diagonals The diagonal to be replaced, i.e. the first,
##' second and so on when looking at the fat version of the matrix
##' (transposed or not) counting from the bottom.
##' Can be a vector to delete more than one diagonal.
##' @return The original matrix with some values missing
##' @author Henning Redestig
deletediagonals <- function(x, diagonals=1) {
wastransposed <- FALSE
if (dim(x)[1] > dim(x)[2]) { # matrix must be lying down
x <- t(x)
wastransposed <- TRUE
}
nr <- nrow(x)
nc <- ncol(x)
if (!all(diagonals <= nc)) {
stop(paste("Order of diagonal number", max(diagonals), "is out of bound"))
}
indexmatrix <- matrix(1 : (nr * nc), ncol=nc, nrow=nr)
finalmatrix <- matrix(ncol=(nr - 1 + nc), nrow=nr)
finalmatrix[,1 : (nr - 1)] <- indexmatrix[,rev((nc : 1)[1 : (nr - 1)])]
finalmatrix[,nr : (nr - 1 + nc)] <- indexmatrix
dia <- 1 + 0:(nr - 1) * (nr + 1)
finalIndices <- NULL
for (i in 1:length(diagonals)) {
indicestodelete <- finalmatrix[dia + (diagonals[i] - 1) * nr]
x[indicestodelete] <- NA
finalIndices <- c(finalIndices, indicestodelete)
}
if (wastransposed) x <- t(x)
return(x)
}
##' Get cross-validation segments that have (as far as possible) the
##' same ratio of all classes (if classes are present)
##' @title Get CV segments
##' @param x a factor, character or numeric vector that describes
##' class membership of a set of items, or, a numeric vector
##' indicating unique indices of items, or, a numeric of length 1 that
##' describes the number of items to segment (without any classes)
##' @param fold the desired number of segments
##' @param seed randomization seed for reproducibility
##' @return a list where each element is a set of indices that defines
##' the CV segment.
##' @examples
##' seg <- cvseg(iris$Species, 10)
##' sapply(seg, function(s) table(iris$Species[s]))
##' cvseg(20, 10)
##' @seealso the \code{cvsegments} function in the \code{pls} package
##' @export
##' @author Henning Redestig
cvseg <- function(x, fold=7, seed=NULL) {
if(any(table(x) > 1)) {
if(any(table(x) < fold)) {
fold <- min(table(x))
}
if(fold < 2)
stop("too few observations in the smallest class")
res <-
sapply(unique(x), function(z) {
if(!is.null(seed))
set.seed(seed)
tmp <- sample(which(x == z))
seg <- matrix(c(tmp,
rep(NA, ifelse(length(tmp) %% fold ==0, 0,
fold - (length(tmp) %% fold)))),
nrow=fold)
},simplify=FALSE)
res <- do.call("cbind", res)
} else {
if(length(x) == 1) x <- 1:x
res <- matrix(sample(c(x,
rep(NA, ifelse(length(x) %% fold ==0, 0,
fold - (length(x) %% fold))))),
nrow=fold)
}
res <- res[!apply(is.na(res), 1, all),,drop=FALSE]
res
lapply(as.data.frame(t(res)), function(x) c(na.omit(x)))
}
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