tests/tmve4.R

dodata <- function(nrep=1, time=FALSE, short=FALSE, full=TRUE, method = c("FASTMVE","MASS")){
##@bdescr
## Test the function covMve() on the literature datasets:
##
## Call covMve() for all regression datasets available in rrco/robustbasev and print:
##  - execution time (if time == TRUE)
##  - objective fucntion
##  - best subsample found (if short == false)
##  - outliers identified (with cutoff 0.975) (if short == false)
##  - estimated center and covarinance matrix if full == TRUE)
##
##@edescr
##
##@in  nrep              : [integer] number of repetitions to use for estimating the
##                                   (average) execution time
##@in  time              : [boolean] whether to evaluate the execution time
##@in  short             : [boolean] whether to do short output (i.e. only the
##                                   objective function value). If short == FALSE,
##                                   the best subsample and the identified outliers are
##                                   printed. See also the parameter full below
##@in  full              : [boolean] whether to print the estimated cente and covariance matrix
##@in  method            : [character] select a method: one of (FASTMCD, MASS)

    domve <- function(x, xname, nrep=1){
        n <- dim(x)[1]
        p <- dim(x)[2]
        alpha <- 0.5
        h <- h.alpha.n(alpha, n, p)
        if(method == "MASS"){
            mve <- cov.mve(x, quantile.used=h)
            quan <- h   #default: floor((n+p+1)/2)
            crit <- mve$crit
            best <- mve$best
            mah <- mahalanobis(x, mve$center, mve$cov)
            quantiel <- qchisq(0.975, p)
            wt <- as.numeric(mah < quantiel)
        }
        else{
            mve <- CovMve(x, trace=FALSE)
            quan <- as.integer(mve@quan)
            crit <- log(mve@crit)
            best <- mve@best
            wt <- mve@wt
        }


        if(time){
           xtime <- system.time(dorep(x, nrep, method))[1]/nrep
           xres <- sprintf("%3d %3d %3d %12.6f %10.3f\n", dim(x)[1], dim(x)[2], quan, crit, xtime)
        }
        else{
            xres <- sprintf("%3d %3d %3d %12.6f\n", dim(x)[1], dim(x)[2], quan, crit)
        }

        lpad<-lname-nchar(xname)
        cat(pad.right(xname,lpad), xres)

        if(!short){
            cat("Best subsample: \n")
            print(best)

            ibad <- which(wt == 0)
            names(ibad) <- NULL
            nbad <- length(ibad)
            cat("Outliers: ", nbad, "\n")
            if(nbad > 0)
                print(ibad)
            if(full){
                cat("-------------\n")
                show(mve)
            }
            cat("--------------------------------------------------------\n")
        }
    }

    options(digits = 5)
    set.seed(101) # <<-- sub-sampling algorithm now based on R's RNG and seed

    lname <- 20

    ## VT::15.09.2013 - this will render the output independent
    ##  from the version of the package
    suppressPackageStartupMessages(library(rrcov))

    method <- match.arg(method)
    if(method == "MASS")
        library(MASS)


    data(heart)
    data(starsCYG)
    data(phosphor)
    data(stackloss)
    data(coleman)
    data(salinity)
    data(wood)

    data(hbk)

    data(Animals, package = "MASS")
    brain <- Animals[c(1:24, 26:25, 27:28),]
    data(milk)
    data(bushfire)

    tmp <- sys.call()
    cat("\nCall: ", deparse(substitute(tmp)),"\n")

    cat("Data Set               n   p  Half LOG(obj)        Time\n")
    cat("========================================================\n")
    domve(heart[, 1:2], data(heart), nrep)
    domve(starsCYG, data(starsCYG), nrep)
    domve(data.matrix(subset(phosphor, select = -plant)), data(phosphor), nrep)
    domve(stack.x, data(stackloss), nrep)
    domve(data.matrix(subset(coleman, select = -Y)), data(coleman), nrep)
    domve(data.matrix(subset(salinity, select = -Y)), data(salinity), nrep)
    domve(data.matrix(subset(wood, select = -y)), data(wood), nrep)
    domve(data.matrix(subset(hbk,  select = -Y)),data(hbk), nrep)

    domve(brain, "Animals", nrep)
    domve(milk, data(milk), nrep)
    domve(bushfire, data(bushfire), nrep)
    cat("========================================================\n")
}

dogen <- function(nrep=1, eps=0.49, method=c("FASTMVE", "MASS")){

    domve <- function(x, nrep=1){
        gc()
        xtime <- system.time(dorep(x, nrep, method))[1]/nrep
        cat(sprintf("%6d %3d %10.2f\n", dim(x)[1], dim(x)[2], xtime))
        xtime
    }

    set.seed(1234)

    ## VT::15.09.2013 - this will render the output independent
    ##  from the version of the package
    suppressPackageStartupMessages(library(rrcov))
    library(MASS)

    method <- match.arg(method)

    ap <- c(2, 5, 10, 20, 30)
    an <- c(100, 500, 1000, 10000, 50000)

    tottime <- 0
    cat("     n   p       Time\n")
    cat("=====================\n")
    for(i in 1:length(an)) {
        for(j in 1:length(ap)) {
            n <- an[i]
            p <- ap[j]
            if(5*p <= n){
                xx <- gendata(n, p, eps)
                X <- xx$X
                tottime <- tottime + domve(X, nrep)
            }
        }
    }

    cat("=====================\n")
    cat("Total time: ", tottime*nrep, "\n")
}

docheck <- function(n, p, eps){
    xx <- gendata(n,p,eps)
    mve <- CovMve(xx$X)
    check(mve, xx$xind)
}

check <- function(mcd, xind){
##  check if mcd is robust w.r.t xind, i.e. check how many of xind
##  did not get zero weight
    mymatch <- xind %in% which(mcd@wt == 0)
    length(xind) - length(which(mymatch))
}

dorep <- function(x, nrep=1, method=c("FASTMVE","MASS")){

    method <- match.arg(method)
    for(i in 1:nrep)
    if(method == "MASS")
        cov.mve(x)
    else
        CovMve(x)
}

#### gendata() ####
# Generates a location contaminated multivariate
# normal sample of n observations in p dimensions
#    (1-eps)*Np(0,Ip) + eps*Np(m,Ip)
# where
#    m = (b,b,...,b)
# Defaults: eps=0 and b=10
#
gendata <- function(n,p,eps=0,b=10){

    if(missing(n) || missing(p))
        stop("Please specify (n,p)")
    if(eps < 0 || eps >= 0.5)
        stop(message="eps must be in [0,0.5)")
    X <- mvrnorm(n,rep(0,p),diag(1,nrow=p,ncol=p))
    nbad <- as.integer(eps * n)
    if(nbad > 0){
        Xbad <- mvrnorm(nbad,rep(b,p),diag(1,nrow=p,ncol=p))
        xind <- sample(n,nbad)
        X[xind,] <- Xbad
    }
    list(X=X, xind=xind)
}

pad.right <- function(z, pads)
{
### Pads spaces to right of text
    padding <- paste(rep(" ", pads), collapse = "")
    paste(z, padding, sep = "")
}

whatis<-function(x){
    if(is.data.frame(x))
        cat("Type: data.frame\n")
    else if(is.matrix(x))
        cat("Type: matrix\n")
    else if(is.vector(x))
        cat("Type: vector\n")
    else
        cat("Type: don't know\n")
}

## VT::15.09.2013 - this will render the output independent
##  from the version of the package
suppressPackageStartupMessages(library(rrcov))

dodata()

Try the rrcov package in your browser

Any scripts or data that you put into this service are public.

rrcov documentation built on July 9, 2023, 6:03 p.m.