\name{iterateBMAsurv.train} \alias{iterateBMAsurv.train} \title{Iterative Bayesian Model Averaging: training} \description{Survival analysis and variable selection on microarray data. This is a multivariate technique to select a small number of relevant variables (typically genes) to perform survival analysis on microarray data. This function performs the training phase. It repeatedly calls \code{bic.surv} from the \code{BMA} package until all variables are exhausted. The variables in the dataset are assumed to be pre-sorted by rank.} \usage{iterateBMAsurv.train (x, surv.time, cens.vec, curr.mat, stopVar=0, nextVar, nbest=10, maxNvar=25, maxIter=200000, thresProbne0=1, verbose = FALSE, suff.string="")} \arguments{ \item{x}{Data matrix where columns are variables and rows are observations. The variables (columns) are assumed to be sorted using a univariate measure. In the case of gene expression data, the columns (variables) represent genes, while the rows (observations) represent samples.} \item{surv.time}{Vector of survival times for the patient samples. Survival times are assumed to be presented in uniform format (e.g., months or days), and the length of this vector should be equal to the number of rows in x.} \item{cens.vec}{Vector of censor data for the patient samples. In general, 0 = censored and 1 = uncensored. The length of this vector should equal the number of rows in x and the number of elements in surv.time.} \item{curr.mat}{Matrix of independent variables in the active \code{bic.surv} window. There can be at most \code{maxNvar} variables in the window at any given time.} \item{stopVar}{0 to continue iterations, 1 to stop iterations (default 0)} \item{nextVar}{Integer placeholder indicating the next variable to be brought into the active \code{bic.surv} window.} \item{nbest}{A number specifying the number of models of each size returned to \code{bic.surv} in the \code{BMA} package. The default is 10.} \item{maxNvar}{A number indicating the maximum number of variables used in each iteration of \code{bic.surv} from the \code{BMA} package. The default is 25.} \item{maxIter}{A number indicating the maximum iterations of \code{bic.surv}. The default is 200000.} \item{thresProbne0}{A number specifying the threshold for the posterior probability that each variable (gene) is non-zero (in percent). Variables (genes) with such posterior probability less than this threshold are dropped in the iterative application of \code{bic.surv}. The default is 1 percent.} \item{verbose}{A boolean variable indicating whether or not to print interim information to the console. The default is FALSE.} \item{suff.string}{A string for writing to file.} } \details{The training phase consists of first ordering all the variables (genes) by a univariate measure such as Cox Proportional Hazards Regression, and then iteratively applying the \code{bic.surv} algorithm from the \code{BMA} package. In the first application of the \code{bic.surv} algorithm, the top \code{maxNvar} univariate ranked genes are used. After each application of the \code{bic.surv} algorithm, the genes with \code{probne0} < \code{thresProbne0} are dropped, and the next univariate ordered genes are added to the active \code{bic.surv} window.} \value{On the last iteration of \code{bic.surv}, four items are returned: \item{curr.mat}{A vector containing the names of the variables (genes) from the final iteration of \code{bic.surv}}. \item{stopVar}{The ending value of stopVar after all iterations.} \item{nextVar}{The ending value of nextVar after all iterations.} \item{}{An object of class \code{bic.surv} resulting from the last iteration of \code{bic.surv}. The object is a list consisting of the following components: \describe{ \item{namesx}{the names of the variables in the last iteration of \code{bic.surv}.} \item{postprob}{the posterior probabilities of the models selected.} \item{label}{labels identifying the models selected.} \item{bic}{values of BIC for the models.} \item{size}{the number of independent variables in each of the models.} \item{which}{a logical matrix with one row per model and one column per variable indicating whether that variable is in the model.} \item{probne0}{the posterior probability that each variable is non-zero (in percent).} \item{postmean}{the posterior mean of each coefficient (from model averaging).} \item{postsd}{the posterior standard deviation of each coefficient (from model averaging).} \item{condpostmean}{the posterior mean of each coefficient conditional on the variable being included in the model.} \item{condpostsd}{the posterior standard deviation of each coefficient conditional on the variable being included in the model.} \item{mle}{matrix with one row per model and one column per variable giving the maximum likelihood estimate of each coefficient for each model.} \item{se}{matrix with one row per model and one column per variable giving the standard error of each coefficient for each model.} \item{reduced}{a logical indicating whether any variables were dropped before model averaging.} \item{dropped}{a vector containing the names of those variables dropped before model averaging.} \item{call}{the matched call that created the bma.lm object.} } } } \references{ Annest, A., Yeung, K.Y., Bumgarner, R.E., and Raftery, A.E. (2008). Iterative Bayesian Model Averaging for Survival Analysis. Manuscript in Progress. Raftery, A.E. (1995). Bayesian model selection in social research (with Discussion). Sociological Methodology 1995 (Peter V. Marsden, ed.), pp. 111-196, Cambridge, Mass.: Blackwells. Volinsky, C., Madigan, D., Raftery, A., and Kronmal, R. (1997) Bayesian Model Averaging in Proprtional Hazard Models: Assessing the Risk of a Stroke. Applied Statistics 46: 433-448. Yeung, K.Y., Bumgarner, R.E. and Raftery, A.E. (2005) Bayesian Model Averaging: Development of an improved multi-class, gene selection and classification tool for microarray data. Bioinformatics 21: 2394-2402. } \note{The \code{BMA} package is required.} \seealso{\code{\link{iterateBMAsurv.train.wrapper}}, \code{\link{iterateBMAsurv.train.predict.assess}}, \code{\link{singleGeneCoxph}}, \code{\link{predictBicSurv}}, \code{\link{trainData}}, \code{\link{trainSurv}}, \code{\link{trainCens}}, \code{\link{testData}} } \examples{ library(BMA) library(iterativeBMAsurv) data(trainData) data(trainSurv) data(trainCens) data(testData) ## Training data should be pre-sorted before beginning ## Initialize the matrix for the active bic.surv window with variables 1 through maxNvar maxNvar <- 25 curr.mat <- trainData[, 1:maxNvar] nextVar <- maxNvar + 1 ## Training phase: select relevant genes using nbest=5 for fast computation ret.bic.surv <- iterateBMAsurv.train (x=trainData, surv.time=trainSurv, cens.vec=trainCens, curr.mat, stopVar=0, nextVar, nbest=5, maxNvar=25) # Apply bic.surv again using selected genes ret.bma <- bic.surv (x=ret.bic.surv$curr.mat, surv.t=trainSurv, cens=trainCens, nbest=5, maxCol=(maxNvar+1)) ## Get the matrix for genes with probne0 > 0 ret.gene.mat <- ret.bic.surv$curr.mat[ret.bma$probne0 > 0] ## Get the gene names from ret.gene.mat selected.genes <- dimnames(ret.gene.mat)[[2]] ## Show the posterior probabilities of selected models ret.bma$postprob ## Get the subset of test data with the genes from the last iteration of ## 'bic.surv' curr.test.dat <- testData[, selected.genes] ## Compute the predicted risk scores for the test samples y.pred.test <- apply (curr.test.dat, 1, predictBicSurv, postprob.vec=ret.bma$postprob, mle.mat=ret.bma$mle) } \keyword{multivariate} \keyword{survival}