Nothing
R/classify.R
In MLSeq: Machine Learning Interface for RNA-Seq Data
Defines functions
classify.discrete
trainNBLDA
trainPLDA
discreteControl
classify.voom
classify.continous
classify
Documented in
classify
discreteControl
globalVariables("ii") ## to remove warnings from 'foreach' package.
#' @include all_generics.R
#' @include voomFunctions.R
#' @title Fitting classification models to sequencing data
#'
#' @description This function fits classification algorithms to sequencing data and measures model performances using various statistics.
#'
#' @details MLSeq consists both microarray-based and discrete-based classifiers along with the preprocessing approaches. These approaches
#' include both normalization techniques, i.e. deseq median ratio (Anders et al., 2010) and trimmed mean of M values (Robinson et al., 2010)
#' normalization methods, and the transformation techniques, i.e. variance- stabilizing transformation (vst)(Anders and Huber, 2010),
#' regularized logarithmic transformation (rlog)(Love et al., 2014), logarithm of counts per million reads (log-cpm)(Robinson et al., 2010)
#' and variance modeling at observational level (voom)(Law et al., 2014). Users can directly upload their raw RNA-Seq count data, preprocess
#' their data, build one of the numerous classification models, optimize the model parameters and evaluate the model performances.
#'
#' MLSeq package consists of a variety of classification algorithms for the classification of RNA-Seq data. These classifiers are
#' categorized into two class: i) microarray-based classifiers after proper transformation, ii) discrete-based classifiers. First option
#' is to transform the RNA-Seq data to bring it hierarchically closer to microarrays and apply microarray-based algorithms. These methods
#' are implemented from the caret package. Run availableMethods() for a list of available methods. Note that voom transformation both
#' exports transformed gene-expression matrix as well as the precision weight matrices in same dimension. Hence, the classifier should
#' consider these two matrices. Zararsiz (2015) presented voom-based diagonal discriminant classifiers and the sparse voom-based nearest
#' shrunken centroids classifier. Second option is to build new discrete-based classifiers to classify RNA-Seq data. Two methods are
#' currently available in the literature. Witten (2011) considered modeling these counts with Poisson distribution and proposed sparse
#' Poisson linear discriminant analysis (PLDA) classifier. The authors suggested a power transformation to deal with the overdispersion
#' problem. Dong et al. (2016) extended this approach into a negative binomial linear discriminant analysis (NBLDA) classifier.
#' More detailed information can be found in referenced papers.
#'
#' @param data a \code{DESeqDataSet} object, see the constructor functions \code{\link[DESeq2:DESeqDataSet]{DESeqDataSet}}, \code{\link[DESeq2:DESeqDataSet]{DESeqDataSetFromMatrix}},
#' \code{\link[DESeq2:DESeqDataSet]{DESeqDataSetFromHTSeqCount}} in DESeq2 package.
#'
#' @param method a character string indicating the name of classification method. Methods are implemented from the \code{caret} package.
#' Run \code{availableMethods()} for a list of available methods.
#'
#' @param normalize a character string indicating the type of normalization. Should be one of 'deseq', 'tmm' and 'none'. Default is 'deseq'. This option
#' should be used with discrete and voom-based classifiers since no transformation is applied on raw counts. For caret-based classifiers,
#' the argument 'preProcessing' should be used.
#'
#' @param preProcessing a character string indicating the name of the preprocessing method. This option consists both the normalization and
#' transformation of the raw sequencing data. Available options are:
#' \itemize{
#' \item \code{deseq-vst}: Normalization is applied with deseq median ratio method. Variance stabiling transformation is applied to the normalized data.
#' \item \code{deseq-rlog}: Normalization is applied with deseq median ratio method. Regularized logarithmic transformation is applied to the normalized data.
#' \item \code{deseq-logcpm}: Normalization is applied with deseq median ratio method. Log of counts-per-million transformation is applied to the normalized data.
#' \item \code{tmm-logcpm}: Normalization is applied with trimmed mean of M values (TMM) method. Log of counts-per-million transformation is applied to the
#' normalized data.
#' \item \code{logcpm}: Normalization is not applied. Log of counts-per-million transformation is used for the raw counts.
#' }
#' \bold{IMPORTANT}: See Details for further information.
#'
#' @param class.labels a character string indicating the column name of colData(...). Should be given as "character". The column from colData()
#' which matches with given column name is used as class labels of samples. If NULL, first column is used as class labels. Default is NULL.
#'
#' @param control a list including all the control parameters passed to model training process. This arguement should be defined using wrapper functions
#' \code{\link[caret]{trainControl}} for caret-based classifiers, \code{\link{discreteControl}} for discrete classifiers (PLDA, PLDA2 and NBLDA) and
#' \code{\link{voomControl}} for voom-based classifiers (voomDLDA, voomDQDA and voomNSC). See related functions for further details.
#'
#' @param B an integer. It is the number of bootstrap samples for bagging classifiers, for example "bagFDA" and "treebag". Default is 25.
#'
#' @param ref a character string indicating the user defined reference class. Default is \code{NULL}. If NULL is selected,
#' first category of class labels is used as reference.
#'
#' @param \dots optional arguments passed to selected classifiers.
#'
#' @return an \code{MLSeq} object for trained model.
#'
#' @author Dincer Goksuluk, Gokmen Zararsiz, Selcuk Korkmaz, Vahap Eldem, Ahmet Ozturk and Ahmet Ergun Karaagaoglu
#'
#' @references
#'
#' Kuhn M. (2008). Building predictive models in R using the caret package. Journal of Statistical Software, (http://www.jstatsoft.org/v28/i05/)
#'
#' Anders S. Huber W. (2010). Differential expression analysis for sequence count data. Genome Biology, 11:R106
#'
#' Witten DM. (2011). Classification and clustering of sequencing data using a poisson model. The Annals of Applied Statistics, 5(4), 2493:2518
#'
#' Law et al. (2014) Voom: precision weights unlock linear model analysis tools for RNA-Seq read counts, Genome Biology, 15:R29, doi:10.1186/gb-2014-15-2-r29
#'
#' Witten D. et al. (2010) Ultra-high throughput sequencing-based small RNA discovery and discrete statistical biomarker analysis in a collection of
#' cervical tumours and matched controls. BMC Biology, 8:58
#'
#' Robinson MD, Oshlack A (2010). A scaling normalization method for differential expression analysis of RNA-Seq data. Genome Biology,
#' 11:R25, doi:10.1186/gb-2010-11-3-r25
#'
#' M. I. Love, W. Huber, and S. Anders (2014). Moderated estimation of fold change and dispersion for rna-seq data with deseq2. Genome Biol,
#' 15(12):550,. doi: 10.1186/s13059-014-0550-8.
#'
#' Dong et al. (2016). NBLDA: negative binomial linear discriminant analysis for rna-seq data. BMC Bioinformatics, 17(1):369, Sep 2016.
#' doi: 10.1186/s12859-016-1208-1.
#'
#' Zararsiz G (2015). Development and Application of Novel Machine Learning Approaches for RNA-Seq Data Classification. PhD thesis,
#' Hacettepe University, Institute of Health Sciences, June 2015.
#'
#' @keywords RNA-seq classification
#'
#' @seealso \code{\link{predictClassify}}, \code{\link[caret]{train}}, \code{\link[caret]{trainControl}},
#' \code{\link{voomControl}}, \code{\link{discreteControl}}
#'
#' @examples
#' \dontrun{
#' library(DESeq2)
#' data(cervical)
#'
#' # a subset of cervical data with first 150 features.
#' data <- cervical[c(1:150), ]
#'
#' # defining sample classes.
#' class <- data.frame(condition = factor(rep(c("N","T"), c(29, 29))))
#'
#' n <- ncol(data) # number of samples
#' p <- nrow(data) # number of features
#'
#' # number of samples for test set (30% test, 70% train).
#' nTest <- ceiling(n*0.3)
#' ind <- sample(n, nTest, FALSE)
#'
#' # train set
#' data.train <- data[ ,-ind]
#' data.train <- as.matrix(data.train + 1)
#' classtr <- data.frame(condition = class[-ind, ])
#'
#' # train set in S4 class
#' data.trainS4 <- DESeqDataSetFromMatrix(countData = data.train,
#' colData = classtr, formula(~ 1))
#'
#' ## Number of repeats (repeats) might change model accuracies
#' ## 1. caret-based classifiers:
#' # Random Forest (RF) Classification
#' rf <- classify(data = data.trainS4, method = "rf",
#' preProcessing = "deseq-vst", ref = "T",
#' control = trainControl(method = "repeatedcv", number = 5,
#' repeats = 2, classProbs = TRUE))
#' rf
#'
#' # 2. Discrete classifiers:
#' # Poisson Linear Discriminant Analysis
#' pmodel <- classify(data = data.trainS4, method = "PLDA", ref = "T",
#' class.labels = "condition",normalize = "deseq",
#' control = discreteControl(number = 5, repeats = 2,
#' tuneLength = 10, parallel = TRUE))
#' pmodel
#'
#' # 3. voom-based classifiers:
#' # voom-based Nearest Shrunken Centroids
#' vmodel <- classify(data = data.trainS4, normalize = "deseq", method = "voomNSC",
#' class.labels = "condition", ref = "T",
#' control = voomControl(number = 5, repeats = 2, tuneLength = 10))
#' vmodel
#' }
#'
#' @name classify
#' @rdname classify
#'
#' @import methods DESeq2 Biobase
#'
#' @importFrom edgeR DGEList calcNormFactors cpm
#' @importFrom stats model.matrix predict relevel xtabs quantile as.dist rexp rnbinom rnorm runif sd
#' @importFrom Biobase ExpressionSet exprs
#' @importFrom limma voom
#' @importFrom caret bagControl confusionMatrix svmBag trainControl bag train
#' @importFrom SummarizedExperiment colData 'colData<-'
#' @importFrom graphics segments
#'
#' @export
classify <- function(data, method = "rpart", B = 25, ref = NULL, class.labels = NULL,
preProcessing = c("deseq-vst", "deseq-rlog", "deseq-logcpm", "tmm-logcpm", "logcpm"),
normalize = c("deseq", "TMM", "none"), control = NULL, ...){
# Define the name of class.labels from DESeqDataSet
if (is.null(class.labels)){
class.labels <- colnames(colData(data))[1]
}
if (!is.null(ref)){
if (!is.character(ref)){
stop("Reference class should be \"character\"")
}
}
# If reference category is not specified, first category is selected as reference category
if (is.null(ref)){
ref = levels(colData(data)[ ,class.labels])[1]
}
# Data class olarak DESeqDataSet'e bagli kalmayalim.
if (class(data)[1] != "DESeqDataSet") {
stop("Data should be a \"DESeqDataSet Object\" of S4 class.")
}
if (is.null(method)){
stop("Classification method is not specified.")
}
if (!(method %in% availableMethods())){
stop("Requested method is not available in \"MLSeq\".")
}
if (method %in% c("voomDLDA", "voomDQDA", "voomNSC")){
## voom-based classifications:
result <- classify.voom(data = data, normalize = normalize, method = method,
class.labels = class.labels, ref = ref, control = control)
} else if (method %in% c("PLDA", "PLDA2", "NBLDA")){
result <- classify.discrete(data = data, method = method, normalize = normalize, ref = ref,
class.labels = class.labels, control = control)
} else {
result <- classify.continous(data, method = method, B = B, ref = ref, class.labels = class.labels,
preProcessing = preProcessing, control = control, ...)
}
return(result)
}
# data = data.trainS4
# method = "svmRadial"
# class.labels = "condition"
# ref = "T"
# preProcessing = "deseq-vst"
# control = trainControl(method = "repeatedcv", number = 5,
# repeats = 2, classProbs = TRUE)
# tuneLength = 15
#' @importFrom caret 'confusionMatrix.train'
classify.continous <- function(data, method = "rpart", B = 25, ref = NULL, class.labels = NULL,
preProcessing = c("deseq-vst", "deseq-rlog", "deseq-logcpm", "tmm-logcpm", "logcpm"),
control = trainControl(method = "repeatedcv", number = 5, repeats = 10), ...){
## Classification function for microarray type classifiers (caret's built-in library is imported here.)
control$controlClass <- "train.control"
call <- match.call()
arg.list <- list(data = data, method = method, B = B, ref = ref, class.labels = class.labels,
preProcessing = preProcessing,
control = control, ...)
rawData <- data
transformedData <- NULL
preProcessing <- match.arg(preProcessing)
if (preProcessing == "deseq-vst"){
normalization <- "deseq"
transformation <- "vst"
dataSF <- estimateSizeFactors(data) # Estimate Size factors:
dataDisp <- estimateDispersions(dataSF, fitType = "local") # Estimate dispersions:
transformedData <- varianceStabilizingTransformation(dataDisp, fitType = "local")
dataVST <- t(as.matrix(assay(transformedData)))
input <- dataVST ## Input data from transformed expression data.
output <- colData(data)[ ,class.labels] ## Output: class labels of samples.
trainParameters <- list(disperFunc = dispersionFunction(dataDisp),
sizeFactors = sizeFactors(dataDisp))
} else if (preProcessing == "deseq-rlog"){
normalization <- "deseq"
transformation <- "rlog"
dataSF <- estimateSizeFactors(data) # Estimate Size factors:
dataDisp <- estimateDispersions(dataSF, fitType = "local") # Estimate dispersions:
transformedData = rlog(dataDisp, blind = FALSE) ### RLOG donusumu uygulanmis olan bu nesnenin de MLSeq objesi icerisinde predictClassify'a gonderilmesi gerekiyor.
dataRLOG = t(assay(transformedData))
input <- dataRLOG ## Input data from transformed expression data.
output <- colData(data)[ ,class.labels] ## Output: class labels of samples.
# dataexpTrainRLOG = t(assay(trS4expRLOG))
# betaPriorVar = attr(trS4expRLOG,"betaPriorVar")
# intercept = mcols(trS4expRLOG)$rlogIntercept
trainParameters <- list(betaPriorVar = attr(dataRLOG,"betaPriorVar"),
intercept = attr(dataRLOG, "intercept"),
dispFit = mcols(transformedData)$dispFit)
} else if (preProcessing == "deseq-logcpm"){
normalization <- "deseq"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "RLE") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
trainParameters <- list(NULL)
} else if (preProcessing == "tmm-logcpm"){
normalization <- "tmm"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "TMM") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
# This function is used to find reference sample.
# Codes are copied from edgeR and modified here.
findRefSample <- function (rawCounts, lib.size, p = 0.75){
y <- t(t(rawCounts) / lib.size)
f75 <- apply(y, 2, function(x){
quantile(x, p = p)
})
refSample <- which.min(abs(f75-mean(f75)))
return(refSample)
}
refSampleID <- findRefSample(rawCounts, lib.size = colSums(rawCounts), p = 0.75)
trainParameters <- list(refSample = rawCounts[ ,refSampleID])
} else if (preProcessing == "logcpm"){
normalization <- "none"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "none") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
trainParameters <- list(NULL)
}
trainedModel <- train(input, output, method = method, trControl = control, ...)
tmp <- confusionMatrix.train(trainedModel, norm = "none")
tbl <- tmp$table / control$repeats
confM = confusionMatrix(round(tbl, 0), positive = ref)
confM$tableRounded <- round(tbl, 2)
confM$table <- round(tbl, 0)
attr(confM, "class") <- "confMat"
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = transformation,
normalization = normalization,
preProcessing = preProcessing,
ref = ref,
control = trainedModel$control,
confusionMat = confM,
trainedModel = trainedModel,
trainParameters = trainParameters,
call = list(call = call, args = arg.list))
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = rawData, transformedData = transformedData))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
result
}
### voom classifiers:
### TODO's
# 1. method argumaninda yer alan runAvailableMethods() fonksiyonunda bir "type" argumani olacak. Bu argumana kisi "voom", "microarray" ...
# girisler yapinca uc farkli classify fonksiyonuna ait methodlar listelenebilecek. setter ve getterlar'da buna gore belirlenecek.
### Classification for voom-based methods.
# data <- data.trainS4
# normalize = "deseq" # c("deseq", "tmm", "none")
# method = "voomNSC" # c("voomNSC", "voomDLDA", "voomDQDA")
# class.labels = "condition"
# ref = "T"
# control = voomControl(number = 3, repeats = 2)
#' @importFrom plyr ldply
classify.voom <- function(data, normalize = c("deseq", "TMM", "none"), method = c("voomNSC", "voomDLDA", "voomDQDA"),
class.labels = NULL, ref = NULL, control = voomControl(), ...){
normalize <- match.arg(normalize)
method <- match.arg(method)
call <- match.call()
arg.list <- list(data = data, normalize = normalize, method = method,
class.labels = class.labels, ref = ref, control = control, ...)
### Calculate train set performances:
folds <- foldIndex(n = nrow(colData(data)), nFolds = control$number, repeats = control$repeats)
## k-fold r-repeat:
# train ve predict işlemleri tüm foldlar ve repeatler için yapılacak.
if (method %in% c("voomDLDA", "voomDQDA")){
# Samples for train in this fold.
counts <- counts(data)
output <- colData(data)[ ,class.labels]
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
input.foldIn <- counts[ ,idx]
output.foldIn <- output[idx]
# Samples for validation in this fold.
input.foldOut <- counts[ ,-idx]
output.foldOut <- output[-idx]
trainResults.fold <- voomDDA.train(input = input.foldIn, output = output.foldIn,
pooled.var = ifelse(method == "voomDLDA", TRUE, FALSE),
normalize = normalize, class.labels = class.labels)
### Predictions for train set:
pred.fold <- factor(predict.voomDDA(object = trainResults.fold, newdata = input.foldOut),
levels = levels(output))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
})
acc <- ldply(lapply(trainResults.AllFolds, function(x)x$accuracies), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
## Final Model
trainedOverall <- voomDDA.train(input = counts(data), output = colData(data)[ ,class.labels],
pooled.var = ifelse(method == "voomDLDA", TRUE, FALSE), normalize = normalize,
class.labels = class.labels)
# predOverall <- factor(predict.voomDDA(object = trainedOverall, newdata = counts(data)))
# tblOverall <- table(Predicted = predOverall, Actual = colData(data)[ ,class.labels])
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(trainResults.AllFolds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
results.tune <- list() ## No tuning results for "voomDLDA" and "voomDQDA"
} else { ### voom NSC calculations:
fit.initial <- voomNSC.train(counts = counts(data), conditions = colData(data)[ ,class.labels],
normalization = normalize, n.threshold = control$tuneLength, getInitialThresholds = FALSE)
initial.thresholds <- fit.initial$threshold
counts <- counts(data)
output <- colData(data)[ ,class.labels]
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
# # Samples for train in this fold.
testdata <- counts[ ,-idx]
test.conditions <- output[-idx]
trainResults.fold <- voomNSC.train(counts = counts, conditions = output,
normalization = normalize, thresholds = initial.thresholds, idxIn = idx)
# ### Predictions for train set:
# pred.fold <- factor(predict.voomNSC(fit = trainResults.fold, newdata = testdata))
# tbl <- table(test.conditions, pred.fold)
# acc.fold <- sum(diag(tbl))/sum(tbl)
#
# return(list(accuracies = acc.fold, predictions = pred.fold))
trainResults.fold[["test.conditions"]] <- test.conditions
return(trainResults.fold)
})
### Find optimum threshold value:
for (i in 1:length(trainResults.AllFolds)){
if (i == 1){
modelResAll <- trainResults.AllFolds[[1]]$modelRes
} else {
modelResAll <- modelResAll + trainResults.AllFolds[[i]]$modelRes
}
}
modelResAll <- modelResAll / length(folds$indexIn)
# opt.threshold.idx <- max(which(modelResAll$avg.errors == min(modelResAll$avg.errors)))
opt.threshold.idx <- max(which(modelResAll$accuracy == max(modelResAll$accuracy)))
opt.threshold <- max(modelResAll$threshold[opt.threshold.idx])
# Return the fold accuracies using optimum thresholds:
acc.Folds <- lapply(trainResults.AllFolds, function(x){
Actual <- x$test.conditions
Preds <- x$predictions[ ,opt.threshold.idx]
tbl <- table(Prediction = Preds, Reference = Actual)
list(errors = x$errors[opt.threshold.idx], predictions = x$predictions[ ,opt.threshold.idx],
accuracy = x$accuracy[opt.threshold.idx], confTables = tbl)
})
acc <- ldply(lapply(acc.Folds, function(x)x$accuracy), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
### BU KISIM PREDICT KISMINA EKLENECEK.
## Confusion Matrix mantığı caret ile benzer şekilde düzenlenecek.
trainedOverall <- voomNSC.train(counts = counts(data), conditions = colData(data)[ ,class.labels],
normalization = normalize, idxIn = NULL, thresholds = opt.threshold)
# trainedOverall <- fit.initial
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(acc.Folds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
results.tune <- list(results = modelResAll, opt.threshold = opt.threshold,
opt.threshold.idx = opt.threshold.idx, overallAccuracy = overallAccuracy)
}
# ## voomTrained adı ile bir S4 class yazılacak.
trainedModel <- new("voom.train",
weigtedStats = trainedOverall$weightedStats,
foldInfo = list(foldAccuracies = acc,
foldPredictions = lapply(trainResults.AllFolds, function(x)x$predictions),
foldIndex = folds),
control = control,
tuningResults = results.tune,
finalModel = list(model = trainedOverall, accuracy = overallAccuracy, finalPredictions = list()),
callInfo = list(method = method, normalize = normalize,
class.labels = class.labels, class.names = as.character(unique(colData(data)[ ,class.labels])),
ref = ref))
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = "voom",
normalization = normalize,
preProcessing = NA_character_,
ref = ref,
control = trainedModel@control,
confusionMat = confM,
trainedModel = trainedModel,
call = list(call = call, args = arg.list))
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = trainedOverall$rawData, transformedData = trainedOverall$transformedData))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
return(result)
}
####### PLDA, NBLDA ##########
#' Define controlling parameters for discrete classifiers (NBLDA and PLDA)
#'
#' This function sets the control parameters for discrete classifiers (PLDA and NBLDA) while training the model.
#'
#' @param method validation method. Support repeated cross validation only ("repeatedcv").
#' @param number a positive integer. Number of folds.
#' @param repeats a positive integer. Number of repeats.
#' @param tuneLength a positive integer. If there is a tuning parameter in the classifier, this value
#' is used to define total number of tuning parameter to be searched.
#' @param rho a single numeric value. This parameter is used as tuning parameter in PLDA classifier.
#' It does not effect NBLDA classifier.
#' @param rhos a numeric vector. If optimum parameter is searched among given values, this option shpould be used.
#' @param beta parameter of Gamma distribution. See PLDA for details.
#' @param prior prior probabilities of each class
#' @param alpha a numeric value in the interval 0 and 1. It is used to apply power transformation through PLDA method.
#' @param truephi a numeric value. If true value of genewise dispersion is known and constant for all genes, this
#' parameter should be used.
#' @param foldIdx a list including the fold indexes. Each element of this list is the vector indices of samples which are
#' used as test set in this fold.
#' @param parallel if TRUE, parallel computing is performed.
#' @param ... further arguments. Deprecated.
#'
#' @author Dincer Goksuluk, Gokmen Zararsiz, Selcuk Korkmaz, Vahap Eldem, Ahmet Ozturk and Ahmet Ergun Karaagaoglu
#'
#' @keywords RNA-seq classification
#'
#' @seealso \code{\link{classify}}, \code{\link[caret]{trainControl}}, \code{\link{discreteControl}}
#'
#' @examples
#' 1L
#'
#' @rdname discreteControl
#'
#' @export
discreteControl <- function(method = "repeatedcv", number = 5, repeats = 10, rho = NULL, rhos = NULL, beta = 1,
prior = NULL, alpha = NULL, truephi = NULL, foldIdx = NULL, tuneLength = 30,
parallel = FALSE, ...){
repeats <- ceiling(repeats)
number <- ceiling(number)
if (is.null(method)){
warning("'method' cannot be NULL. It is set to 'repeatedcv'.")
method <- "repeatedcv"
}
if (method != "repeatedcv"){
warning("Currently, only 'repeatedcv' is supported for model training. 'method' is set to 'repeatedcv'.")
method <- "repeatedcv"
}
if (number <= 0){
stop("'number' must be positive integer.")
}
if (repeats <= 0){
stop("'repeats' must be positive integer.")
}
if (!is.null(rho)){
if (any(rho < 0)){
stop("'rho' cannot be negative value.")
}
if (length(rho) >= 2){
warning("A single value should be given for 'rho'. Only the first element is used.")
rho <- rho[1]
}
}
if (!is.null(rhos) && any(rhos < 0)){
stop("'rhos' cannot be negative value.")
}
if (!is.null(prior) && (any(prior > 1) || any(prior < 0))){
stop("'prior' should be between 0 and 1.")
}
if (tuneLength <= 0){
stop("'tuneLength' must be positive integer and non-zero.")
}
if (!is.null(alpha)){
if (length(alpha >= 2)){
warning("A single value should be given for 'alpha'. Only the first element is used.")
alpha <- alpha[1]
}
if (alpha < 0 || alpha > 1){
stop("'alpha' should be between 0 and 1.")
}
}
list(method = method, number = number, repeats = repeats, rho = rho, rhos = rhos, beta = beta,
prior = prior, alpha = alpha, truephi = truephi, foldIdx = foldIdx, tuneLength = tuneLength,
parallel = parallel, controlClass = "discrete.control", ...)
}
#' @importFrom foreach foreach '%do%' '%dopar%'
#' @importFrom utils globalVariables
trainPLDA <- function(x, y, rhos = NULL, beta = 1, type = c("mle", "deseq", "quantile", "none", "TMM"),
folds = NULL, transform = TRUE, alpha = NULL, prior = NULL, nfolds = 5, repeats = 10,
tuneLength = 10, parallel = FALSE, ...){
# This function performs cross-validation to find the optimum value of tuning parameter "rho"
# Args:
# x: A n-by-p training data matrix; n observations and p features. Used to train the classifier.
# y: A numeric vector of class labels of length n: 1, 2, ...., K if there are K classes.
# Each element of y corresponds to a row of x; i.e. these are the class labels for the observations in x.
# rhos: A vector of tuning parameters that control the amount of soft thresholding performed. If "rhos" is
# provided then a number of models will be fit (one for each element of "rhos"), and a number of
# predicted class labels will be output (one for each element of "rhos").
# beta: A smoothing term. A Gamma(beta,beta) prior is used to fit the Poisson model.
# Recommendation is to just leave it at 1, the default value.
# nfolds: The number of folds in the cross-validation; default is 5-fold cross-validation.
# type: How should the observations be normalized within the Poisson model, i.e. how should the size factors be estimated?
# Options are "quantile" or "deseq" (more robust) or "mle" (less robust).
# In greater detail: "quantile" is quantile normalization approach of Bullard et al 2010 BMC Bioinformatics
# "deseq" is median of the ratio of an observation to a pseudoreference obtained by taking the geometric mean,
# described in Anders and Huber 2010 Genome Biology and implemented in Bioconductor package "DESeq", and "mle" is the
# sum of counts for each sample; this is the maximum likelihood estimate under a simple Poisson model.
# folds: Instead of specifying the number of folds in cross-validation, one can explicitly specify the folds. To do this,
# input a list of length r (to perform r-fold cross-validation). The rth element of the list should be a vector
# containing the indices of the test observations in the rth fold.
# transform: Should data matrices x and xte first be power transformed so that it more closely fits the Poisson model?
# TRUE or FALSE. Power transformation is especially useful if the data are overdispersed relative to the Poisson model.
# alpha: If transform=TRUE, this determines the power to which the data matrices x and xte are transformed. If alpha = NULL then
# the transformation that makes the Poisson model best fit the data matrix x is computed. (Note that alpha is computed
# based on x, not based on xte). Or a value of alpha, 0<alpha<=1, can be entered by the user.
# prior: Vector of length equal to the number of classes, representing prior probabilities for each class. If NULL then
# uniform priors are used (i.e. each class is equally likely).
# ii <- NULL
if (!transform && !is.null(alpha)) stop("You have asked for NO transformation but have entered alpha.")
if (transform && is.null(alpha)) alpha <- FindBestTransform(x)
## Apply power transform here.
if (transform){
if (alpha <= 0 || alpha > 1){
stop("alpha must be between 0 and 1")
}
x <- x^alpha
}
if (is.null(rhos)){
ns <- NullModel(x, type = type)$n ## Normalized counts.
uniq <- sort(unique(y))
maxrho <- rep(NA, length(uniq))
for (k in 1:length(uniq)){
a <- colSums(x[y == uniq[k], ]) + beta
b <- colSums(ns[y == uniq[k], ]) + beta
maxrho[k] <- max(abs(a/b - 1)*sqrt(b), na.rm = TRUE)
}
rhos <- seq(0, max(maxrho, na.rm = TRUE)*(2/3), len = tuneLength) ## len will be included in the control arguement as "tuneLength"
}
### f-fold r-repeats fold indices.
if (is.null(folds)){
foldIdx <- lapply(1:repeats, function(u){
tmp.fold <- balanced.folds(y, nfolds = nfolds)
names(tmp.fold) <- paste("Fold.", 1:length(tmp.fold), sep = "")
tmp.fold
})
names(foldIdx) <- paste("Repeat.", 1:repeats, sep = "")
} else {
foldIdx <- folds
}
### FOREACH ILE PARALEL KODLAMA:
# c("rhos", "x", "y", "beta", "prior", "Classify",
# "NullModel", "NullModelTest", "GetD", "Soft", "foldIdx")
if (parallel){
nn <- length(foldIdx)
foldResults <- foreach(ii = 1:nn, .inorder = TRUE, .multicombine = TRUE,
.export = c("Classify", "NullModel", "NullModelTest", "GetD", "Soft")) %dopar% {
f <- foldIdx[[ii]] # ii.th repeat
nfolds <- length(f) # number of folds in ii.th repeat
errs <- nnonzero <- accuracy <- matrix(NA, nrow = nfolds, ncol = length(rhos))
confusionTables.fold <- confusionTables.fold.rho <- list()
for (i in 1:nfolds){ ### loop for each fold within ii'th repeat
tr <- -f[[i]]
te <- f[[i]]
# Type olarak neden sadece "quantile" üzerinden classify edilmiş??
out <- Classify(x[tr, ], y[tr], x[te, ], rhos = rhos, beta = beta,
type = "quantile", prior = prior, transform = FALSE) # Have already power-transformed x, so don't need to do it again!!!
for (j in 1:length(rhos)){
errs[i, j] <- sum(out[[j]]$ytehat != y[te])
nnonzero[i, j] <- sum(colSums(out[[j]]$ds != 1) != 0)
accuracy[i, j] <- (length(y[te]) - sum(out[[j]]$ytehat != y[te])) / length(y[te])
confusionTables.fold.rho[[j]] <- table(Prediction = out[[j]]$ytehat, Reference = y[te])
}
names(confusionTables.fold.rho) <- paste0("rho.", rhos)
confusionTables.fold[[i]] <- confusionTables.fold.rho
}
names(confusionTables.fold) <- paste0("Fold.", 1:nfolds)
return(list(errs = errs, nnonzero = nnonzero, accuracy = accuracy, rhos = rhos, confTables = confusionTables.fold))
}
names(foldResults) <- paste("Repeat.", 1:length(foldResults), sep = "")
} else {
nn <- length(foldIdx)
foldResults <- foreach(ii = 1:nn, .inorder = TRUE, .multicombine = TRUE,
.export = c("Classify", "NullModel", "NullModelTest", "GetD", "Soft")) %do% {
f <- foldIdx[[ii]]
nfolds <- length(f)
errs <- nnonzero <- accuracy <- matrix(NA, nrow = nfolds, ncol = length(rhos))
confusionTables.fold <- confusionTables.fold.rho <- list()
for (i in 1:nfolds){
tr <- -f[[i]]
te <- f[[i]]
# Type olarak neden sadece "quantile" üzerinden classify edilmiş??
out <- Classify(x[tr, ], y[tr], x[te, ], rhos = rhos, beta = beta,
type = "quantile", prior = prior, transform = FALSE) # Have already power-transformed x, so don't need to do it again!!!
for (j in 1:length(rhos)){
errs[i, j] <- sum(out[[j]]$ytehat != y[te])
nnonzero[i, j] <- sum(colSums(out[[j]]$ds != 1) != 0)
accuracy[i, j] <- (length(y[te]) - sum(out[[j]]$ytehat != y[te])) / length(y[te])
confusionTables.fold.rho[[j]] <- table(Prediction = out[[j]]$ytehat, Reference = y[te])
}
confusionTables.fold[[i]] <- confusionTables.fold.rho
}
names(confusionTables.fold) <- paste0("Fold.", 1:nfolds)
return(list(errs = errs, nnonzero = nnonzero, accuracy = accuracy, rhos = rhos, confTables = confusionTables.fold))
}
names(foldResults) <- paste("Repeat.", 1:length(foldResults), sep = "")
}
### Accuracy and non-zero features avaraged over repeated folds.
errs.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$errs)
}), "rbind", .id = NULL))
nnonzero.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$nnonzero)
}), "rbind", .id = NULL))
acc.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$accuracy)
}), "rbind", .id = NULL))
tuneResults <- data.frame(rho = rhos, Avg.Error = errs.average, Avg.NonZeroFeat. = nnonzero.average, Accuracy = acc.average)
idx <- max(which(acc.average == max(acc.average)))
bestrho <- rhos[idx]
bestAccuracy <- tuneResults[idx, "Accuracy"]
bestNonZeroFeat <- tuneResults[idx, "Avg.NonZeroFeat."]
# tuneResults <- as.matrix(tuneResults)
## BURADA PLDA için yazılmış olan sınıfa göre bir S4 sonuç dönecek.
## discrete.train
res <- list(inputs = list(x = x, y = y, x.test = NULL, y.test = NULL), control = list(foldIdx = foldIdx),
tuningResults = list(rhos = rhos, bestrho = bestrho, bestrho.idx = idx, bestAccuracy = bestAccuracy,
bestNonZeroFeat = bestNonZeroFeat, results = tuneResults, alpha.transform = alpha),
selectedGenes = NULL,
foldResults = foldResults)
return(res)
}
#' @importFrom sSeq getT getAdjustDisp rowVars
trainNBLDA <- function(x, y, xte = NULL, beta = 1, type = c("mle", "deseq", "quantile", "none", "TMM"),
prior = NULL, truephi = NULL, ...){
# Args:
# x: a data.frame or matrix with counts. Samples are in the rows and genes are in the columns.
# y: a vector (numeric or factor) including the class labels of each subject.
# xte: a data frame or matrix of test samples. If NULL, train set is used as test set.
# beta:
# type:
# prior:
# truephi:
if (is.null(prior)){
prior <- rep(1/length(unique(y)), length(unique(y)))
## prior vectorunun sinif sayisi ile esit uzunlukta olmasi lazım.
## Bu durumu kontrol edip gerekirse uyari verilecek.
}
null.out <- NullModel(x, type = type)
ns <- null.out$n
nste <- NullModelTest(null.out, x, xte, type = type)$nste
uniq <- sort(unique(y))
ds <- GetDnb(ns, x, y, beta)
## Dispersion estimates.
if (!is.null(truephi)){
if (length(truephi) >= 2 & (length(truephi) != ncol(ns))){
truephi <- truephi[1]
disperhat <- rep(truephi, ncol(ns))
warning("The length of \"truephi\" should be the same as number of features. Only the first element is used and replicated for all features.")
} else if (length(truephi) == 1){
disperhat <- rep(truephi, ncol(ns))
} else if (length(truephi) >= 2 & (length(truephi) == ncol(ns))){
disperhat <- truephi
}
} else {
####### TO DO #######
# tt değerinin 0'a eşit olması durumu ile analiz yapılıyor ama normalde üstteki değere shrink ediliyor. Yu et al çalışmasındaki gibi.
# Bunun nedeni araştırılacak. 0 Değerini almak problem yaratır mı diye incelenecek.
tt <- getT(t(x), sizeFactors = rep(1, nrow(x)), verbose = FALSE, propForSigma = c(0, 1))$target
### Moment estimation of gene-wise dispersions.
rM = rowMeans(t(x))
rV = rowVars(t(x))
disp = (rV - rM)/rM^2 ## Dispersion estimates using method-of-moments.
# disp0 = numeric()
## Negative dispersions are set to 0.
disp0 <- sapply(disp, function(x){
max(0, x)
})
disperhat <- getAdjustDisp(disp0, shrinkTarget = tt, verbose = FALSE)$adj
disperhat <- pmax(rep(0, length(disperhat)), disperhat) ## Negative dispersions are set to 0.
}
# if (!is.null(truephi)){
# if (length(truephi) >= 2){
# truephi <- truephi[1]
# warning("\"truephi\" should be given as a single value. Only first element is used.")
# }
# disperhat <- rep(truephi, ncol(nste))
#
# } else {
# tt = getT(t(x), sizeFactors = rep(1, nrow(x)), verbose = FALSE)$target
#
# ### Moment estimation of gene-wise dispersions.
# rM = rowMeans(t(x))
# rV = rowVars(t(x))
#
# disp = (rV - rM)/rM^2
# disp0 = numeric()
#
# for (i in 1:length(disp)){
# a1 = 0
# a2 = disp[i]
# disp0[i] = max(a1, a2) ## Negative dispersions are set to 0.
# }
# names(disp0) <- names(disp)
#
# disperhat = getAdjustDisp(disp0, shrinkTarget = tt, verbose = FALSE)$adj
# }
phihat <- as.numeric(disperhat)
discriminant <- matrix(NA, nrow = nrow(xte), ncol = length(uniq))
# Replace Infinity with zero dispersions.
inv.phihat <- (1/phihat)
if (any(inv.phihat == Inf | inv.phihat == -Inf)){
id.inf <- which(inv.phihat == Inf | inv.phihat == -Inf)
inv.phihat[id.inf] <- 0
} else {
id.inf <- NULL
}
for (k in 1:length(uniq)){
for (l in 1:nrow(xte)){
dstar = ds[k, ]
part2 = 1 + nste[l, ] * dstar * phihat
part1 = dstar/part2
part3 <- (1/phihat) * log(part2)
if (!is.null(id.inf)){
part3.limits <- nste[l, ] * dstar
part3[id.inf] <- part3.limits[id.inf]
}
discriminant[l, k]<- sum(xte[l, ] * log(part1)) - sum(part3) + log(prior[k])
}
}
preds <- uniq[apply(discriminant, 1, which.max)] ## Predicted class labels.
result <- structure(list(ns = ns, nste = nste, ds = ds, discriminant = discriminant,
ytehat = preds, x = x, y = y, xte = xte, type = type,
disp = disperhat, null.out = null.out),
class = "list")
return(result)
}
# #
# data <- data.trainS4
# method = "NBLDA" # c("PLDA", "PLDA2", "NBLDA")
# normalize = "deseq" # c("deseq", "TMM", "none")
# ref = "T"
# class.labels = "condition"
# control = discreteControl(number = 5, repeats = 1, tuneLength = 10, parallel = TRUE)
# type <- normalize
## Discrete classifiers: PLDA, PLDA2, NBLDA
## data: a DESeqDataSet object.
classify.discrete <- function(data, method = c("PLDA", "PLDA2", "NBLDA"), normalize = c("deseq", "TMM", "none"),
ref = NULL, class.labels = NULL, control = discreteControl(), ...){
call <- match.call()
arg.list <- list(data = data, method = method, normalize = normalize,
ref = ref, class.labels = class.labels, control = control, ...)
# extract arguements from control list.
rho <- control$rho
rhos <- control$rhos
beta <- control$beta
prior <- control$prior
alpha <- control$alpha
folds <- control$foldIdx
tuneLength <- control$tuneLength
# size factor estimation method. should be one of "deseq", "TMM" and "none"
type <- match.arg(normalize)
method <- match.arg(method)
transform <- FALSE
if (method == "PLDA2") transform <- TRUE ### PLDA2 is used fr power transformed PLDA.
# Raw counts from DESeqDataSet object. Samples in the rows and genes in the columns.
x <- t(counts(data))
# Class labels.
y <- colData(data)[ ,class.labels]
if (method %in% c("PLDA", "PLDA2")){
model.fit <- trainPLDA(x, y, rhos = rhos, beta = beta, nfolds = control$number, repeats = control$repeats, type = type,
folds = folds, transform = transform, alpha = alpha, prior = prior, tuneLength = tuneLength, parallel = control$parallel)
# # CONFUSION MATRIX MANTIGI CARET ILE BENZER OLACAK
model.fit.final <- if (transform){
Classify(x, y, xte = x, rho = model.fit$tuningResults$bestrho, beta = beta, rhos = NULL,
type = type, prior = prior, transform = TRUE,
alpha = model.fit$tuningResults$alpha.transform)
} else {
Classify(x, y, xte = x, rho = model.fit$tuningResults$bestrho, beta = beta, rhos = NULL,
type = type, prior = prior, transform = FALSE)
}
# export "control" list into plda train object.
if (is.null(control$foldIdx)){
fold.idx <- model.fit$control$foldIdx
model.fit$control <- control
model.fit$control$foldIdx <- fold.idx
} else {
model.fit$control <- control
}
# bestrho kullanılarak train set yeniden train edilerek modele seçilen genlerin isimleri belirlenecek.
# Bu genler selectedFeatures olarak train objesi içerisinde verilecek.
ds <- model.fit.final$ds
selectedGenesIdx <- which(!apply(ds == 1, 2, all))
selectedGenesNames <- colnames(x)[selectedGenesIdx]
if (model.fit$tuningResults$bestrho != 0){
model.fit.final$SelectedGenes <- list(selectedGenesIdx = selectedGenesIdx, selectedGenesNames = selectedGenesNames)
} else {
model.fit.final$SelectedGenes <- list(selectedGenesIdx = NULL, selectedGenesNames = NULL)
}
### Confusion matrix daha sonra overall predicted values üzerinden düzenlenecek. Aggregated over folds.
### Confusion matrix "caret" mantığı ile veriliyor. Bütün repeat ve fold'lara ait classification table'lar
### kullanılarak bir aggregated sonuç verilecek.
bestrho.index <- model.fit$tuningResults$bestrho.idx
aggregatedTable <- unlist(lapply(model.fit$foldResults, function(x){
tmp <- x$confTables
lapply(tmp, function(y){
y[[bestrho.index]]
})
}), recursive = FALSE)
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
## BURADA ELDE EDILEN DEGERLER TAMSAYI OLMADIGI DURUMDA HATA VERIYOR. BU SEBEPLE OVERALL DEGERLERIN
## KULLANILMASI DAHA UYGUNDUR. ANCAK ELDE EDILEN SONUCLARDAKI P-DEGERLERI VE GUVEN ARALIKLARININ
## DIKKATE ALINMAMASI GEREKIYOR. BU BILGININ BIR NOT OLARAK VERILMESI UYGUN OLABILIR.
tmp <- tmp / model.fit$control$repeats
tmp.attr <- attributes(tmp)
names(tmp.attr$dimnames) <- c("Prediction", "Reference")
attributes(tmp) <- tmp.attr
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
} else if (method == "NBLDA"){
### Calculate train set performances using repeated cross-validation:
folds <- foldIndex(n = nrow(colData(data)), nFolds = control$number, repeats = control$repeats)
parallel <- control$parallel
if (parallel){
nn <- length(folds$indexIn)
fold.tmp <- folds$indexIn
trainResults.AllFolds <- foreach(i = 1:nn, .inorder = FALSE, .multicombine = TRUE,
.export = c("NullModel", "NullModelTest", "GetDnb", "Soft",
"trainNBLDA", "x", "y", "fold.tmp", "type")) %dopar% {
idx <- fold.tmp[[i]]
input.foldIn <- x[idx, ]
output.foldIn <- y[idx]
# Samples for validation in this fold.
input.foldOut <- x[-idx, ]
output.foldOut <- y[-idx]
trainResults.fold <- trainNBLDA(x = input.foldIn, y = output.foldIn, xte = input.foldOut, type = type)
### Predictions for train set:
pred.fold <- factor(trainResults.fold$ytehat, levels = levels(y))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
}
names(trainResults.AllFolds) <- names(folds$indexIn)
} else {
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
input.foldIn <- x[idx, ]
output.foldIn <- y[idx]
# Samples for validation in this fold.
input.foldOut <- x[-idx, ]
output.foldOut <- y[-idx]
trainResults.fold <- trainNBLDA(x = input.foldIn, y = output.foldIn, xte = input.foldOut, type = type)
### Predictions for train set:
pred.fold <- factor(trainResults.fold$ytehat, levels = levels(y))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
})
}
acc <- ldply(lapply(trainResults.AllFolds, function(x)x$accuracies), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
## Final Model
trainedOverall <- trainNBLDA(x = t(counts(data)), y = colData(data)[ ,class.labels], xte = x, type = normalize)
model.fit <- trainedOverall
model.fit[["tuningResults"]] <- list()
model.fit.final <- model.fit
model.fit.final[["overallAccuracy"]] <- overallAccuracy
model.fit.final[["trainParameters"]] <- model.fit$null.out
control$foldIdx <- folds
model.fit[["control"]] <- control
model.fit[["inputs"]] <- list(x = model.fit$x, y = model.fit$y)
model.fit[["foldInfo"]] <- list(foldAccuracies = acc,
foldPredictions = lapply(trainResults.AllFolds, function(x)x$predictions),
foldIndex = folds)
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(trainResults.AllFolds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
}
# ## discrete.train adı ile bir S4 class yazılacak.
trainedModel <- new("discrete.train",
inputs = model.fit$inputs,
control = model.fit$control,
crossValidatedModel = model.fit,
tuningResults = model.fit$tuningResults,
finalModel = model.fit.final,
callInfo = list(method = method, normalize = normalize,
class.labels = class.labels, class.names = as.character(unique(colData(data)[ ,class.labels])),
ref = ref))
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = NA_character_,
normalization = normalize,
preProcessing = NA_character_,
ref = ref,
control = trainedModel@control, ## PLDA'da kullanılan discreteControl(...) objesi
confusionMat = confM, ## Cross-validated confusion matrix
trainedModel = trainedModel,
trainParameters = trainedModel@finalModel$trainParameters,
call = list(call = call, args = arg.list))
if (transform){
transformedData <- model.fit.final$x
} else {
transformedData <- NULL
}
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = x, transformedData = transformedData, conditions = y))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
return(result)
}
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Defines functions classify.discrete trainNBLDA trainPLDA discreteControl classify.voom classify.continous classify
Documented in classify discreteControl
globalVariables("ii") ## to remove warnings from 'foreach' package.
#' @include all_generics.R
#' @include voomFunctions.R
#' @title Fitting classification models to sequencing data
#'
#' @description This function fits classification algorithms to sequencing data and measures model performances using various statistics.
#'
#' @details MLSeq consists both microarray-based and discrete-based classifiers along with the preprocessing approaches. These approaches
#' include both normalization techniques, i.e. deseq median ratio (Anders et al., 2010) and trimmed mean of M values (Robinson et al., 2010)
#' normalization methods, and the transformation techniques, i.e. variance- stabilizing transformation (vst)(Anders and Huber, 2010),
#' regularized logarithmic transformation (rlog)(Love et al., 2014), logarithm of counts per million reads (log-cpm)(Robinson et al., 2010)
#' and variance modeling at observational level (voom)(Law et al., 2014). Users can directly upload their raw RNA-Seq count data, preprocess
#' their data, build one of the numerous classification models, optimize the model parameters and evaluate the model performances.
#'
#' MLSeq package consists of a variety of classification algorithms for the classification of RNA-Seq data. These classifiers are
#' categorized into two class: i) microarray-based classifiers after proper transformation, ii) discrete-based classifiers. First option
#' is to transform the RNA-Seq data to bring it hierarchically closer to microarrays and apply microarray-based algorithms. These methods
#' are implemented from the caret package. Run availableMethods() for a list of available methods. Note that voom transformation both
#' exports transformed gene-expression matrix as well as the precision weight matrices in same dimension. Hence, the classifier should
#' consider these two matrices. Zararsiz (2015) presented voom-based diagonal discriminant classifiers and the sparse voom-based nearest
#' shrunken centroids classifier. Second option is to build new discrete-based classifiers to classify RNA-Seq data. Two methods are
#' currently available in the literature. Witten (2011) considered modeling these counts with Poisson distribution and proposed sparse
#' Poisson linear discriminant analysis (PLDA) classifier. The authors suggested a power transformation to deal with the overdispersion
#' problem. Dong et al. (2016) extended this approach into a negative binomial linear discriminant analysis (NBLDA) classifier.
#' More detailed information can be found in referenced papers.
#'
#' @param data a \code{DESeqDataSet} object, see the constructor functions \code{\link[DESeq2:DESeqDataSet]{DESeqDataSet}}, \code{\link[DESeq2:DESeqDataSet]{DESeqDataSetFromMatrix}},
#' \code{\link[DESeq2:DESeqDataSet]{DESeqDataSetFromHTSeqCount}} in DESeq2 package.
#'
#' @param method a character string indicating the name of classification method. Methods are implemented from the \code{caret} package.
#' Run \code{availableMethods()} for a list of available methods.
#'
#' @param normalize a character string indicating the type of normalization. Should be one of 'deseq', 'tmm' and 'none'. Default is 'deseq'. This option
#' should be used with discrete and voom-based classifiers since no transformation is applied on raw counts. For caret-based classifiers,
#' the argument 'preProcessing' should be used.
#'
#' @param preProcessing a character string indicating the name of the preprocessing method. This option consists both the normalization and
#' transformation of the raw sequencing data. Available options are:
#' \itemize{
#' \item \code{deseq-vst}: Normalization is applied with deseq median ratio method. Variance stabiling transformation is applied to the normalized data.
#' \item \code{deseq-rlog}: Normalization is applied with deseq median ratio method. Regularized logarithmic transformation is applied to the normalized data.
#' \item \code{deseq-logcpm}: Normalization is applied with deseq median ratio method. Log of counts-per-million transformation is applied to the normalized data.
#' \item \code{tmm-logcpm}: Normalization is applied with trimmed mean of M values (TMM) method. Log of counts-per-million transformation is applied to the
#' normalized data.
#' \item \code{logcpm}: Normalization is not applied. Log of counts-per-million transformation is used for the raw counts.
#' }
#' \bold{IMPORTANT}: See Details for further information.
#'
#' @param class.labels a character string indicating the column name of colData(...). Should be given as "character". The column from colData()
#' which matches with given column name is used as class labels of samples. If NULL, first column is used as class labels. Default is NULL.
#'
#' @param control a list including all the control parameters passed to model training process. This arguement should be defined using wrapper functions
#' \code{\link[caret]{trainControl}} for caret-based classifiers, \code{\link{discreteControl}} for discrete classifiers (PLDA, PLDA2 and NBLDA) and
#' \code{\link{voomControl}} for voom-based classifiers (voomDLDA, voomDQDA and voomNSC). See related functions for further details.
#'
#' @param B an integer. It is the number of bootstrap samples for bagging classifiers, for example "bagFDA" and "treebag". Default is 25.
#'
#' @param ref a character string indicating the user defined reference class. Default is \code{NULL}. If NULL is selected,
#' first category of class labels is used as reference.
#'
#' @param \dots optional arguments passed to selected classifiers.
#'
#' @return an \code{MLSeq} object for trained model.
#'
#' @author Dincer Goksuluk, Gokmen Zararsiz, Selcuk Korkmaz, Vahap Eldem, Ahmet Ozturk and Ahmet Ergun Karaagaoglu
#'
#' @references
#'
#' Kuhn M. (2008). Building predictive models in R using the caret package. Journal of Statistical Software, (http://www.jstatsoft.org/v28/i05/)
#'
#' Anders S. Huber W. (2010). Differential expression analysis for sequence count data. Genome Biology, 11:R106
#'
#' Witten DM. (2011). Classification and clustering of sequencing data using a poisson model. The Annals of Applied Statistics, 5(4), 2493:2518
#'
#' Law et al. (2014) Voom: precision weights unlock linear model analysis tools for RNA-Seq read counts, Genome Biology, 15:R29, doi:10.1186/gb-2014-15-2-r29
#'
#' Witten D. et al. (2010) Ultra-high throughput sequencing-based small RNA discovery and discrete statistical biomarker analysis in a collection of
#' cervical tumours and matched controls. BMC Biology, 8:58
#'
#' Robinson MD, Oshlack A (2010). A scaling normalization method for differential expression analysis of RNA-Seq data. Genome Biology,
#' 11:R25, doi:10.1186/gb-2010-11-3-r25
#'
#' M. I. Love, W. Huber, and S. Anders (2014). Moderated estimation of fold change and dispersion for rna-seq data with deseq2. Genome Biol,
#' 15(12):550,. doi: 10.1186/s13059-014-0550-8.
#'
#' Dong et al. (2016). NBLDA: negative binomial linear discriminant analysis for rna-seq data. BMC Bioinformatics, 17(1):369, Sep 2016.
#' doi: 10.1186/s12859-016-1208-1.
#'
#' Zararsiz G (2015). Development and Application of Novel Machine Learning Approaches for RNA-Seq Data Classification. PhD thesis,
#' Hacettepe University, Institute of Health Sciences, June 2015.
#'
#' @keywords RNA-seq classification
#'
#' @seealso \code{\link{predictClassify}}, \code{\link[caret]{train}}, \code{\link[caret]{trainControl}},
#' \code{\link{voomControl}}, \code{\link{discreteControl}}
#'
#' @examples
#' \dontrun{
#' library(DESeq2)
#' data(cervical)
#'
#' # a subset of cervical data with first 150 features.
#' data <- cervical[c(1:150), ]
#'
#' # defining sample classes.
#' class <- data.frame(condition = factor(rep(c("N","T"), c(29, 29))))
#'
#' n <- ncol(data) # number of samples
#' p <- nrow(data) # number of features
#'
#' # number of samples for test set (30% test, 70% train).
#' nTest <- ceiling(n*0.3)
#' ind <- sample(n, nTest, FALSE)
#'
#' # train set
#' data.train <- data[ ,-ind]
#' data.train <- as.matrix(data.train + 1)
#' classtr <- data.frame(condition = class[-ind, ])
#'
#' # train set in S4 class
#' data.trainS4 <- DESeqDataSetFromMatrix(countData = data.train,
#' colData = classtr, formula(~ 1))
#'
#' ## Number of repeats (repeats) might change model accuracies
#' ## 1. caret-based classifiers:
#' # Random Forest (RF) Classification
#' rf <- classify(data = data.trainS4, method = "rf",
#' preProcessing = "deseq-vst", ref = "T",
#' control = trainControl(method = "repeatedcv", number = 5,
#' repeats = 2, classProbs = TRUE))
#' rf
#'
#' # 2. Discrete classifiers:
#' # Poisson Linear Discriminant Analysis
#' pmodel <- classify(data = data.trainS4, method = "PLDA", ref = "T",
#' class.labels = "condition",normalize = "deseq",
#' control = discreteControl(number = 5, repeats = 2,
#' tuneLength = 10, parallel = TRUE))
#' pmodel
#'
#' # 3. voom-based classifiers:
#' # voom-based Nearest Shrunken Centroids
#' vmodel <- classify(data = data.trainS4, normalize = "deseq", method = "voomNSC",
#' class.labels = "condition", ref = "T",
#' control = voomControl(number = 5, repeats = 2, tuneLength = 10))
#' vmodel
#' }
#'
#' @name classify
#' @rdname classify
#'
#' @import methods DESeq2 Biobase
#'
#' @importFrom edgeR DGEList calcNormFactors cpm
#' @importFrom stats model.matrix predict relevel xtabs quantile as.dist rexp rnbinom rnorm runif sd
#' @importFrom Biobase ExpressionSet exprs
#' @importFrom limma voom
#' @importFrom caret bagControl confusionMatrix svmBag trainControl bag train
#' @importFrom SummarizedExperiment colData 'colData<-'
#' @importFrom graphics segments
#'
#' @export
classify <- function(data, method = "rpart", B = 25, ref = NULL, class.labels = NULL,
preProcessing = c("deseq-vst", "deseq-rlog", "deseq-logcpm", "tmm-logcpm", "logcpm"),
normalize = c("deseq", "TMM", "none"), control = NULL, ...){
# Define the name of class.labels from DESeqDataSet
if (is.null(class.labels)){
class.labels <- colnames(colData(data))[1]
}
if (!is.null(ref)){
if (!is.character(ref)){
stop("Reference class should be \"character\"")
}
}
# If reference category is not specified, first category is selected as reference category
if (is.null(ref)){
ref = levels(colData(data)[ ,class.labels])[1]
}
# Data class olarak DESeqDataSet'e bagli kalmayalim.
if (class(data)[1] != "DESeqDataSet") {
stop("Data should be a \"DESeqDataSet Object\" of S4 class.")
}
if (is.null(method)){
stop("Classification method is not specified.")
}
if (!(method %in% availableMethods())){
stop("Requested method is not available in \"MLSeq\".")
}
if (method %in% c("voomDLDA", "voomDQDA", "voomNSC")){
## voom-based classifications:
result <- classify.voom(data = data, normalize = normalize, method = method,
class.labels = class.labels, ref = ref, control = control)
} else if (method %in% c("PLDA", "PLDA2", "NBLDA")){
result <- classify.discrete(data = data, method = method, normalize = normalize, ref = ref,
class.labels = class.labels, control = control)
} else {
result <- classify.continous(data, method = method, B = B, ref = ref, class.labels = class.labels,
preProcessing = preProcessing, control = control, ...)
}
return(result)
}
# data = data.trainS4
# method = "svmRadial"
# class.labels = "condition"
# ref = "T"
# preProcessing = "deseq-vst"
# control = trainControl(method = "repeatedcv", number = 5,
# repeats = 2, classProbs = TRUE)
# tuneLength = 15
#' @importFrom caret 'confusionMatrix.train'
classify.continous <- function(data, method = "rpart", B = 25, ref = NULL, class.labels = NULL,
preProcessing = c("deseq-vst", "deseq-rlog", "deseq-logcpm", "tmm-logcpm", "logcpm"),
control = trainControl(method = "repeatedcv", number = 5, repeats = 10), ...){
## Classification function for microarray type classifiers (caret's built-in library is imported here.)
control$controlClass <- "train.control"
call <- match.call()
arg.list <- list(data = data, method = method, B = B, ref = ref, class.labels = class.labels,
preProcessing = preProcessing,
control = control, ...)
rawData <- data
transformedData <- NULL
preProcessing <- match.arg(preProcessing)
if (preProcessing == "deseq-vst"){
normalization <- "deseq"
transformation <- "vst"
dataSF <- estimateSizeFactors(data) # Estimate Size factors:
dataDisp <- estimateDispersions(dataSF, fitType = "local") # Estimate dispersions:
transformedData <- varianceStabilizingTransformation(dataDisp, fitType = "local")
dataVST <- t(as.matrix(assay(transformedData)))
input <- dataVST ## Input data from transformed expression data.
output <- colData(data)[ ,class.labels] ## Output: class labels of samples.
trainParameters <- list(disperFunc = dispersionFunction(dataDisp),
sizeFactors = sizeFactors(dataDisp))
} else if (preProcessing == "deseq-rlog"){
normalization <- "deseq"
transformation <- "rlog"
dataSF <- estimateSizeFactors(data) # Estimate Size factors:
dataDisp <- estimateDispersions(dataSF, fitType = "local") # Estimate dispersions:
transformedData = rlog(dataDisp, blind = FALSE) ### RLOG donusumu uygulanmis olan bu nesnenin de MLSeq objesi icerisinde predictClassify'a gonderilmesi gerekiyor.
dataRLOG = t(assay(transformedData))
input <- dataRLOG ## Input data from transformed expression data.
output <- colData(data)[ ,class.labels] ## Output: class labels of samples.
# dataexpTrainRLOG = t(assay(trS4expRLOG))
# betaPriorVar = attr(trS4expRLOG,"betaPriorVar")
# intercept = mcols(trS4expRLOG)$rlogIntercept
trainParameters <- list(betaPriorVar = attr(dataRLOG,"betaPriorVar"),
intercept = attr(dataRLOG, "intercept"),
dispFit = mcols(transformedData)$dispFit)
} else if (preProcessing == "deseq-logcpm"){
normalization <- "deseq"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "RLE") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
trainParameters <- list(NULL)
} else if (preProcessing == "tmm-logcpm"){
normalization <- "tmm"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "TMM") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
# This function is used to find reference sample.
# Codes are copied from edgeR and modified here.
findRefSample <- function (rawCounts, lib.size, p = 0.75){
y <- t(t(rawCounts) / lib.size)
f75 <- apply(y, 2, function(x){
quantile(x, p = p)
})
refSample <- which.min(abs(f75-mean(f75)))
return(refSample)
}
refSampleID <- findRefSample(rawCounts, lib.size = colSums(rawCounts), p = 0.75)
trainParameters <- list(refSample = rawCounts[ ,refSampleID])
} else if (preProcessing == "logcpm"){
normalization <- "none"
transformation <- "logcpm"
rawCounts = counts(data, normalized = FALSE)
countsDGE <- DGEList(counts = rawCounts, genes = rownames(rawCounts))
countsDGE.normalized <- calcNormFactors(countsDGE, method = "none") ## RLE: DESeq mantigi ile normalize ediyor.
countsDGE.transformed <- cpm(countsDGE.normalized, log = TRUE, prior.count = 1) ### prior Count daha sonra duzenlenecek.
rawData <- countsDGE
classes <- colData(data)[ ,class.labels]
rawData[[class.labels]] <- classes
transformedData <- list(normalizedData = countsDGE.normalized, transformedData = countsDGE.transformed)
transformedData[[class.labels]] <- classes
input <- t(countsDGE.transformed) ## Input data from transformed expression data.
output <- rawData[[class.labels]] ## Output: class labels of samples.
trainParameters <- list(NULL)
}
trainedModel <- train(input, output, method = method, trControl = control, ...)
tmp <- confusionMatrix.train(trainedModel, norm = "none")
tbl <- tmp$table / control$repeats
confM = confusionMatrix(round(tbl, 0), positive = ref)
confM$tableRounded <- round(tbl, 2)
confM$table <- round(tbl, 0)
attr(confM, "class") <- "confMat"
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = transformation,
normalization = normalization,
preProcessing = preProcessing,
ref = ref,
control = trainedModel$control,
confusionMat = confM,
trainedModel = trainedModel,
trainParameters = trainParameters,
call = list(call = call, args = arg.list))
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = rawData, transformedData = transformedData))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
result
}
### voom classifiers:
### TODO's
# 1. method argumaninda yer alan runAvailableMethods() fonksiyonunda bir "type" argumani olacak. Bu argumana kisi "voom", "microarray" ...
# girisler yapinca uc farkli classify fonksiyonuna ait methodlar listelenebilecek. setter ve getterlar'da buna gore belirlenecek.
### Classification for voom-based methods.
# data <- data.trainS4
# normalize = "deseq" # c("deseq", "tmm", "none")
# method = "voomNSC" # c("voomNSC", "voomDLDA", "voomDQDA")
# class.labels = "condition"
# ref = "T"
# control = voomControl(number = 3, repeats = 2)
#' @importFrom plyr ldply
classify.voom <- function(data, normalize = c("deseq", "TMM", "none"), method = c("voomNSC", "voomDLDA", "voomDQDA"),
class.labels = NULL, ref = NULL, control = voomControl(), ...){
normalize <- match.arg(normalize)
method <- match.arg(method)
call <- match.call()
arg.list <- list(data = data, normalize = normalize, method = method,
class.labels = class.labels, ref = ref, control = control, ...)
### Calculate train set performances:
folds <- foldIndex(n = nrow(colData(data)), nFolds = control$number, repeats = control$repeats)
## k-fold r-repeat:
# train ve predict işlemleri tüm foldlar ve repeatler için yapılacak.
if (method %in% c("voomDLDA", "voomDQDA")){
# Samples for train in this fold.
counts <- counts(data)
output <- colData(data)[ ,class.labels]
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
input.foldIn <- counts[ ,idx]
output.foldIn <- output[idx]
# Samples for validation in this fold.
input.foldOut <- counts[ ,-idx]
output.foldOut <- output[-idx]
trainResults.fold <- voomDDA.train(input = input.foldIn, output = output.foldIn,
pooled.var = ifelse(method == "voomDLDA", TRUE, FALSE),
normalize = normalize, class.labels = class.labels)
### Predictions for train set:
pred.fold <- factor(predict.voomDDA(object = trainResults.fold, newdata = input.foldOut),
levels = levels(output))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
})
acc <- ldply(lapply(trainResults.AllFolds, function(x)x$accuracies), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
## Final Model
trainedOverall <- voomDDA.train(input = counts(data), output = colData(data)[ ,class.labels],
pooled.var = ifelse(method == "voomDLDA", TRUE, FALSE), normalize = normalize,
class.labels = class.labels)
# predOverall <- factor(predict.voomDDA(object = trainedOverall, newdata = counts(data)))
# tblOverall <- table(Predicted = predOverall, Actual = colData(data)[ ,class.labels])
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(trainResults.AllFolds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
results.tune <- list() ## No tuning results for "voomDLDA" and "voomDQDA"
} else { ### voom NSC calculations:
fit.initial <- voomNSC.train(counts = counts(data), conditions = colData(data)[ ,class.labels],
normalization = normalize, n.threshold = control$tuneLength, getInitialThresholds = FALSE)
initial.thresholds <- fit.initial$threshold
counts <- counts(data)
output <- colData(data)[ ,class.labels]
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
# # Samples for train in this fold.
testdata <- counts[ ,-idx]
test.conditions <- output[-idx]
trainResults.fold <- voomNSC.train(counts = counts, conditions = output,
normalization = normalize, thresholds = initial.thresholds, idxIn = idx)
# ### Predictions for train set:
# pred.fold <- factor(predict.voomNSC(fit = trainResults.fold, newdata = testdata))
# tbl <- table(test.conditions, pred.fold)
# acc.fold <- sum(diag(tbl))/sum(tbl)
#
# return(list(accuracies = acc.fold, predictions = pred.fold))
trainResults.fold[["test.conditions"]] <- test.conditions
return(trainResults.fold)
})
### Find optimum threshold value:
for (i in 1:length(trainResults.AllFolds)){
if (i == 1){
modelResAll <- trainResults.AllFolds[[1]]$modelRes
} else {
modelResAll <- modelResAll + trainResults.AllFolds[[i]]$modelRes
}
}
modelResAll <- modelResAll / length(folds$indexIn)
# opt.threshold.idx <- max(which(modelResAll$avg.errors == min(modelResAll$avg.errors)))
opt.threshold.idx <- max(which(modelResAll$accuracy == max(modelResAll$accuracy)))
opt.threshold <- max(modelResAll$threshold[opt.threshold.idx])
# Return the fold accuracies using optimum thresholds:
acc.Folds <- lapply(trainResults.AllFolds, function(x){
Actual <- x$test.conditions
Preds <- x$predictions[ ,opt.threshold.idx]
tbl <- table(Prediction = Preds, Reference = Actual)
list(errors = x$errors[opt.threshold.idx], predictions = x$predictions[ ,opt.threshold.idx],
accuracy = x$accuracy[opt.threshold.idx], confTables = tbl)
})
acc <- ldply(lapply(acc.Folds, function(x)x$accuracy), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
### BU KISIM PREDICT KISMINA EKLENECEK.
## Confusion Matrix mantığı caret ile benzer şekilde düzenlenecek.
trainedOverall <- voomNSC.train(counts = counts(data), conditions = colData(data)[ ,class.labels],
normalization = normalize, idxIn = NULL, thresholds = opt.threshold)
# trainedOverall <- fit.initial
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(acc.Folds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
results.tune <- list(results = modelResAll, opt.threshold = opt.threshold,
opt.threshold.idx = opt.threshold.idx, overallAccuracy = overallAccuracy)
}
# ## voomTrained adı ile bir S4 class yazılacak.
trainedModel <- new("voom.train",
weigtedStats = trainedOverall$weightedStats,
foldInfo = list(foldAccuracies = acc,
foldPredictions = lapply(trainResults.AllFolds, function(x)x$predictions),
foldIndex = folds),
control = control,
tuningResults = results.tune,
finalModel = list(model = trainedOverall, accuracy = overallAccuracy, finalPredictions = list()),
callInfo = list(method = method, normalize = normalize,
class.labels = class.labels, class.names = as.character(unique(colData(data)[ ,class.labels])),
ref = ref))
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = "voom",
normalization = normalize,
preProcessing = NA_character_,
ref = ref,
control = trainedModel@control,
confusionMat = confM,
trainedModel = trainedModel,
call = list(call = call, args = arg.list))
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = trainedOverall$rawData, transformedData = trainedOverall$transformedData))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
return(result)
}
####### PLDA, NBLDA ##########
#' Define controlling parameters for discrete classifiers (NBLDA and PLDA)
#'
#' This function sets the control parameters for discrete classifiers (PLDA and NBLDA) while training the model.
#'
#' @param method validation method. Support repeated cross validation only ("repeatedcv").
#' @param number a positive integer. Number of folds.
#' @param repeats a positive integer. Number of repeats.
#' @param tuneLength a positive integer. If there is a tuning parameter in the classifier, this value
#' is used to define total number of tuning parameter to be searched.
#' @param rho a single numeric value. This parameter is used as tuning parameter in PLDA classifier.
#' It does not effect NBLDA classifier.
#' @param rhos a numeric vector. If optimum parameter is searched among given values, this option shpould be used.
#' @param beta parameter of Gamma distribution. See PLDA for details.
#' @param prior prior probabilities of each class
#' @param alpha a numeric value in the interval 0 and 1. It is used to apply power transformation through PLDA method.
#' @param truephi a numeric value. If true value of genewise dispersion is known and constant for all genes, this
#' parameter should be used.
#' @param foldIdx a list including the fold indexes. Each element of this list is the vector indices of samples which are
#' used as test set in this fold.
#' @param parallel if TRUE, parallel computing is performed.
#' @param ... further arguments. Deprecated.
#'
#' @author Dincer Goksuluk, Gokmen Zararsiz, Selcuk Korkmaz, Vahap Eldem, Ahmet Ozturk and Ahmet Ergun Karaagaoglu
#'
#' @keywords RNA-seq classification
#'
#' @seealso \code{\link{classify}}, \code{\link[caret]{trainControl}}, \code{\link{discreteControl}}
#'
#' @examples
#' 1L
#'
#' @rdname discreteControl
#'
#' @export
discreteControl <- function(method = "repeatedcv", number = 5, repeats = 10, rho = NULL, rhos = NULL, beta = 1,
prior = NULL, alpha = NULL, truephi = NULL, foldIdx = NULL, tuneLength = 30,
parallel = FALSE, ...){
repeats <- ceiling(repeats)
number <- ceiling(number)
if (is.null(method)){
warning("'method' cannot be NULL. It is set to 'repeatedcv'.")
method <- "repeatedcv"
}
if (method != "repeatedcv"){
warning("Currently, only 'repeatedcv' is supported for model training. 'method' is set to 'repeatedcv'.")
method <- "repeatedcv"
}
if (number <= 0){
stop("'number' must be positive integer.")
}
if (repeats <= 0){
stop("'repeats' must be positive integer.")
}
if (!is.null(rho)){
if (any(rho < 0)){
stop("'rho' cannot be negative value.")
}
if (length(rho) >= 2){
warning("A single value should be given for 'rho'. Only the first element is used.")
rho <- rho[1]
}
}
if (!is.null(rhos) && any(rhos < 0)){
stop("'rhos' cannot be negative value.")
}
if (!is.null(prior) && (any(prior > 1) || any(prior < 0))){
stop("'prior' should be between 0 and 1.")
}
if (tuneLength <= 0){
stop("'tuneLength' must be positive integer and non-zero.")
}
if (!is.null(alpha)){
if (length(alpha >= 2)){
warning("A single value should be given for 'alpha'. Only the first element is used.")
alpha <- alpha[1]
}
if (alpha < 0 || alpha > 1){
stop("'alpha' should be between 0 and 1.")
}
}
list(method = method, number = number, repeats = repeats, rho = rho, rhos = rhos, beta = beta,
prior = prior, alpha = alpha, truephi = truephi, foldIdx = foldIdx, tuneLength = tuneLength,
parallel = parallel, controlClass = "discrete.control", ...)
}
#' @importFrom foreach foreach '%do%' '%dopar%'
#' @importFrom utils globalVariables
trainPLDA <- function(x, y, rhos = NULL, beta = 1, type = c("mle", "deseq", "quantile", "none", "TMM"),
folds = NULL, transform = TRUE, alpha = NULL, prior = NULL, nfolds = 5, repeats = 10,
tuneLength = 10, parallel = FALSE, ...){
# This function performs cross-validation to find the optimum value of tuning parameter "rho"
# Args:
# x: A n-by-p training data matrix; n observations and p features. Used to train the classifier.
# y: A numeric vector of class labels of length n: 1, 2, ...., K if there are K classes.
# Each element of y corresponds to a row of x; i.e. these are the class labels for the observations in x.
# rhos: A vector of tuning parameters that control the amount of soft thresholding performed. If "rhos" is
# provided then a number of models will be fit (one for each element of "rhos"), and a number of
# predicted class labels will be output (one for each element of "rhos").
# beta: A smoothing term. A Gamma(beta,beta) prior is used to fit the Poisson model.
# Recommendation is to just leave it at 1, the default value.
# nfolds: The number of folds in the cross-validation; default is 5-fold cross-validation.
# type: How should the observations be normalized within the Poisson model, i.e. how should the size factors be estimated?
# Options are "quantile" or "deseq" (more robust) or "mle" (less robust).
# In greater detail: "quantile" is quantile normalization approach of Bullard et al 2010 BMC Bioinformatics
# "deseq" is median of the ratio of an observation to a pseudoreference obtained by taking the geometric mean,
# described in Anders and Huber 2010 Genome Biology and implemented in Bioconductor package "DESeq", and "mle" is the
# sum of counts for each sample; this is the maximum likelihood estimate under a simple Poisson model.
# folds: Instead of specifying the number of folds in cross-validation, one can explicitly specify the folds. To do this,
# input a list of length r (to perform r-fold cross-validation). The rth element of the list should be a vector
# containing the indices of the test observations in the rth fold.
# transform: Should data matrices x and xte first be power transformed so that it more closely fits the Poisson model?
# TRUE or FALSE. Power transformation is especially useful if the data are overdispersed relative to the Poisson model.
# alpha: If transform=TRUE, this determines the power to which the data matrices x and xte are transformed. If alpha = NULL then
# the transformation that makes the Poisson model best fit the data matrix x is computed. (Note that alpha is computed
# based on x, not based on xte). Or a value of alpha, 0<alpha<=1, can be entered by the user.
# prior: Vector of length equal to the number of classes, representing prior probabilities for each class. If NULL then
# uniform priors are used (i.e. each class is equally likely).
# ii <- NULL
if (!transform && !is.null(alpha)) stop("You have asked for NO transformation but have entered alpha.")
if (transform && is.null(alpha)) alpha <- FindBestTransform(x)
## Apply power transform here.
if (transform){
if (alpha <= 0 || alpha > 1){
stop("alpha must be between 0 and 1")
}
x <- x^alpha
}
if (is.null(rhos)){
ns <- NullModel(x, type = type)$n ## Normalized counts.
uniq <- sort(unique(y))
maxrho <- rep(NA, length(uniq))
for (k in 1:length(uniq)){
a <- colSums(x[y == uniq[k], ]) + beta
b <- colSums(ns[y == uniq[k], ]) + beta
maxrho[k] <- max(abs(a/b - 1)*sqrt(b), na.rm = TRUE)
}
rhos <- seq(0, max(maxrho, na.rm = TRUE)*(2/3), len = tuneLength) ## len will be included in the control arguement as "tuneLength"
}
### f-fold r-repeats fold indices.
if (is.null(folds)){
foldIdx <- lapply(1:repeats, function(u){
tmp.fold <- balanced.folds(y, nfolds = nfolds)
names(tmp.fold) <- paste("Fold.", 1:length(tmp.fold), sep = "")
tmp.fold
})
names(foldIdx) <- paste("Repeat.", 1:repeats, sep = "")
} else {
foldIdx <- folds
}
### FOREACH ILE PARALEL KODLAMA:
# c("rhos", "x", "y", "beta", "prior", "Classify",
# "NullModel", "NullModelTest", "GetD", "Soft", "foldIdx")
if (parallel){
nn <- length(foldIdx)
foldResults <- foreach(ii = 1:nn, .inorder = TRUE, .multicombine = TRUE,
.export = c("Classify", "NullModel", "NullModelTest", "GetD", "Soft")) %dopar% {
f <- foldIdx[[ii]] # ii.th repeat
nfolds <- length(f) # number of folds in ii.th repeat
errs <- nnonzero <- accuracy <- matrix(NA, nrow = nfolds, ncol = length(rhos))
confusionTables.fold <- confusionTables.fold.rho <- list()
for (i in 1:nfolds){ ### loop for each fold within ii'th repeat
tr <- -f[[i]]
te <- f[[i]]
# Type olarak neden sadece "quantile" üzerinden classify edilmiş??
out <- Classify(x[tr, ], y[tr], x[te, ], rhos = rhos, beta = beta,
type = "quantile", prior = prior, transform = FALSE) # Have already power-transformed x, so don't need to do it again!!!
for (j in 1:length(rhos)){
errs[i, j] <- sum(out[[j]]$ytehat != y[te])
nnonzero[i, j] <- sum(colSums(out[[j]]$ds != 1) != 0)
accuracy[i, j] <- (length(y[te]) - sum(out[[j]]$ytehat != y[te])) / length(y[te])
confusionTables.fold.rho[[j]] <- table(Prediction = out[[j]]$ytehat, Reference = y[te])
}
names(confusionTables.fold.rho) <- paste0("rho.", rhos)
confusionTables.fold[[i]] <- confusionTables.fold.rho
}
names(confusionTables.fold) <- paste0("Fold.", 1:nfolds)
return(list(errs = errs, nnonzero = nnonzero, accuracy = accuracy, rhos = rhos, confTables = confusionTables.fold))
}
names(foldResults) <- paste("Repeat.", 1:length(foldResults), sep = "")
} else {
nn <- length(foldIdx)
foldResults <- foreach(ii = 1:nn, .inorder = TRUE, .multicombine = TRUE,
.export = c("Classify", "NullModel", "NullModelTest", "GetD", "Soft")) %do% {
f <- foldIdx[[ii]]
nfolds <- length(f)
errs <- nnonzero <- accuracy <- matrix(NA, nrow = nfolds, ncol = length(rhos))
confusionTables.fold <- confusionTables.fold.rho <- list()
for (i in 1:nfolds){
tr <- -f[[i]]
te <- f[[i]]
# Type olarak neden sadece "quantile" üzerinden classify edilmiş??
out <- Classify(x[tr, ], y[tr], x[te, ], rhos = rhos, beta = beta,
type = "quantile", prior = prior, transform = FALSE) # Have already power-transformed x, so don't need to do it again!!!
for (j in 1:length(rhos)){
errs[i, j] <- sum(out[[j]]$ytehat != y[te])
nnonzero[i, j] <- sum(colSums(out[[j]]$ds != 1) != 0)
accuracy[i, j] <- (length(y[te]) - sum(out[[j]]$ytehat != y[te])) / length(y[te])
confusionTables.fold.rho[[j]] <- table(Prediction = out[[j]]$ytehat, Reference = y[te])
}
confusionTables.fold[[i]] <- confusionTables.fold.rho
}
names(confusionTables.fold) <- paste0("Fold.", 1:nfolds)
return(list(errs = errs, nnonzero = nnonzero, accuracy = accuracy, rhos = rhos, confTables = confusionTables.fold))
}
names(foldResults) <- paste("Repeat.", 1:length(foldResults), sep = "")
}
### Accuracy and non-zero features avaraged over repeated folds.
errs.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$errs)
}), "rbind", .id = NULL))
nnonzero.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$nnonzero)
}), "rbind", .id = NULL))
acc.average <- colMeans(plyr::ldply(lapply(foldResults, function(u){
colMeans(u$accuracy)
}), "rbind", .id = NULL))
tuneResults <- data.frame(rho = rhos, Avg.Error = errs.average, Avg.NonZeroFeat. = nnonzero.average, Accuracy = acc.average)
idx <- max(which(acc.average == max(acc.average)))
bestrho <- rhos[idx]
bestAccuracy <- tuneResults[idx, "Accuracy"]
bestNonZeroFeat <- tuneResults[idx, "Avg.NonZeroFeat."]
# tuneResults <- as.matrix(tuneResults)
## BURADA PLDA için yazılmış olan sınıfa göre bir S4 sonuç dönecek.
## discrete.train
res <- list(inputs = list(x = x, y = y, x.test = NULL, y.test = NULL), control = list(foldIdx = foldIdx),
tuningResults = list(rhos = rhos, bestrho = bestrho, bestrho.idx = idx, bestAccuracy = bestAccuracy,
bestNonZeroFeat = bestNonZeroFeat, results = tuneResults, alpha.transform = alpha),
selectedGenes = NULL,
foldResults = foldResults)
return(res)
}
#' @importFrom sSeq getT getAdjustDisp rowVars
trainNBLDA <- function(x, y, xte = NULL, beta = 1, type = c("mle", "deseq", "quantile", "none", "TMM"),
prior = NULL, truephi = NULL, ...){
# Args:
# x: a data.frame or matrix with counts. Samples are in the rows and genes are in the columns.
# y: a vector (numeric or factor) including the class labels of each subject.
# xte: a data frame or matrix of test samples. If NULL, train set is used as test set.
# beta:
# type:
# prior:
# truephi:
if (is.null(prior)){
prior <- rep(1/length(unique(y)), length(unique(y)))
## prior vectorunun sinif sayisi ile esit uzunlukta olmasi lazım.
## Bu durumu kontrol edip gerekirse uyari verilecek.
}
null.out <- NullModel(x, type = type)
ns <- null.out$n
nste <- NullModelTest(null.out, x, xte, type = type)$nste
uniq <- sort(unique(y))
ds <- GetDnb(ns, x, y, beta)
## Dispersion estimates.
if (!is.null(truephi)){
if (length(truephi) >= 2 & (length(truephi) != ncol(ns))){
truephi <- truephi[1]
disperhat <- rep(truephi, ncol(ns))
warning("The length of \"truephi\" should be the same as number of features. Only the first element is used and replicated for all features.")
} else if (length(truephi) == 1){
disperhat <- rep(truephi, ncol(ns))
} else if (length(truephi) >= 2 & (length(truephi) == ncol(ns))){
disperhat <- truephi
}
} else {
####### TO DO #######
# tt değerinin 0'a eşit olması durumu ile analiz yapılıyor ama normalde üstteki değere shrink ediliyor. Yu et al çalışmasındaki gibi.
# Bunun nedeni araştırılacak. 0 Değerini almak problem yaratır mı diye incelenecek.
tt <- getT(t(x), sizeFactors = rep(1, nrow(x)), verbose = FALSE, propForSigma = c(0, 1))$target
### Moment estimation of gene-wise dispersions.
rM = rowMeans(t(x))
rV = rowVars(t(x))
disp = (rV - rM)/rM^2 ## Dispersion estimates using method-of-moments.
# disp0 = numeric()
## Negative dispersions are set to 0.
disp0 <- sapply(disp, function(x){
max(0, x)
})
disperhat <- getAdjustDisp(disp0, shrinkTarget = tt, verbose = FALSE)$adj
disperhat <- pmax(rep(0, length(disperhat)), disperhat) ## Negative dispersions are set to 0.
}
# if (!is.null(truephi)){
# if (length(truephi) >= 2){
# truephi <- truephi[1]
# warning("\"truephi\" should be given as a single value. Only first element is used.")
# }
# disperhat <- rep(truephi, ncol(nste))
#
# } else {
# tt = getT(t(x), sizeFactors = rep(1, nrow(x)), verbose = FALSE)$target
#
# ### Moment estimation of gene-wise dispersions.
# rM = rowMeans(t(x))
# rV = rowVars(t(x))
#
# disp = (rV - rM)/rM^2
# disp0 = numeric()
#
# for (i in 1:length(disp)){
# a1 = 0
# a2 = disp[i]
# disp0[i] = max(a1, a2) ## Negative dispersions are set to 0.
# }
# names(disp0) <- names(disp)
#
# disperhat = getAdjustDisp(disp0, shrinkTarget = tt, verbose = FALSE)$adj
# }
phihat <- as.numeric(disperhat)
discriminant <- matrix(NA, nrow = nrow(xte), ncol = length(uniq))
# Replace Infinity with zero dispersions.
inv.phihat <- (1/phihat)
if (any(inv.phihat == Inf | inv.phihat == -Inf)){
id.inf <- which(inv.phihat == Inf | inv.phihat == -Inf)
inv.phihat[id.inf] <- 0
} else {
id.inf <- NULL
}
for (k in 1:length(uniq)){
for (l in 1:nrow(xte)){
dstar = ds[k, ]
part2 = 1 + nste[l, ] * dstar * phihat
part1 = dstar/part2
part3 <- (1/phihat) * log(part2)
if (!is.null(id.inf)){
part3.limits <- nste[l, ] * dstar
part3[id.inf] <- part3.limits[id.inf]
}
discriminant[l, k]<- sum(xte[l, ] * log(part1)) - sum(part3) + log(prior[k])
}
}
preds <- uniq[apply(discriminant, 1, which.max)] ## Predicted class labels.
result <- structure(list(ns = ns, nste = nste, ds = ds, discriminant = discriminant,
ytehat = preds, x = x, y = y, xte = xte, type = type,
disp = disperhat, null.out = null.out),
class = "list")
return(result)
}
# #
# data <- data.trainS4
# method = "NBLDA" # c("PLDA", "PLDA2", "NBLDA")
# normalize = "deseq" # c("deseq", "TMM", "none")
# ref = "T"
# class.labels = "condition"
# control = discreteControl(number = 5, repeats = 1, tuneLength = 10, parallel = TRUE)
# type <- normalize
## Discrete classifiers: PLDA, PLDA2, NBLDA
## data: a DESeqDataSet object.
classify.discrete <- function(data, method = c("PLDA", "PLDA2", "NBLDA"), normalize = c("deseq", "TMM", "none"),
ref = NULL, class.labels = NULL, control = discreteControl(), ...){
call <- match.call()
arg.list <- list(data = data, method = method, normalize = normalize,
ref = ref, class.labels = class.labels, control = control, ...)
# extract arguements from control list.
rho <- control$rho
rhos <- control$rhos
beta <- control$beta
prior <- control$prior
alpha <- control$alpha
folds <- control$foldIdx
tuneLength <- control$tuneLength
# size factor estimation method. should be one of "deseq", "TMM" and "none"
type <- match.arg(normalize)
method <- match.arg(method)
transform <- FALSE
if (method == "PLDA2") transform <- TRUE ### PLDA2 is used fr power transformed PLDA.
# Raw counts from DESeqDataSet object. Samples in the rows and genes in the columns.
x <- t(counts(data))
# Class labels.
y <- colData(data)[ ,class.labels]
if (method %in% c("PLDA", "PLDA2")){
model.fit <- trainPLDA(x, y, rhos = rhos, beta = beta, nfolds = control$number, repeats = control$repeats, type = type,
folds = folds, transform = transform, alpha = alpha, prior = prior, tuneLength = tuneLength, parallel = control$parallel)
# # CONFUSION MATRIX MANTIGI CARET ILE BENZER OLACAK
model.fit.final <- if (transform){
Classify(x, y, xte = x, rho = model.fit$tuningResults$bestrho, beta = beta, rhos = NULL,
type = type, prior = prior, transform = TRUE,
alpha = model.fit$tuningResults$alpha.transform)
} else {
Classify(x, y, xte = x, rho = model.fit$tuningResults$bestrho, beta = beta, rhos = NULL,
type = type, prior = prior, transform = FALSE)
}
# export "control" list into plda train object.
if (is.null(control$foldIdx)){
fold.idx <- model.fit$control$foldIdx
model.fit$control <- control
model.fit$control$foldIdx <- fold.idx
} else {
model.fit$control <- control
}
# bestrho kullanılarak train set yeniden train edilerek modele seçilen genlerin isimleri belirlenecek.
# Bu genler selectedFeatures olarak train objesi içerisinde verilecek.
ds <- model.fit.final$ds
selectedGenesIdx <- which(!apply(ds == 1, 2, all))
selectedGenesNames <- colnames(x)[selectedGenesIdx]
if (model.fit$tuningResults$bestrho != 0){
model.fit.final$SelectedGenes <- list(selectedGenesIdx = selectedGenesIdx, selectedGenesNames = selectedGenesNames)
} else {
model.fit.final$SelectedGenes <- list(selectedGenesIdx = NULL, selectedGenesNames = NULL)
}
### Confusion matrix daha sonra overall predicted values üzerinden düzenlenecek. Aggregated over folds.
### Confusion matrix "caret" mantığı ile veriliyor. Bütün repeat ve fold'lara ait classification table'lar
### kullanılarak bir aggregated sonuç verilecek.
bestrho.index <- model.fit$tuningResults$bestrho.idx
aggregatedTable <- unlist(lapply(model.fit$foldResults, function(x){
tmp <- x$confTables
lapply(tmp, function(y){
y[[bestrho.index]]
})
}), recursive = FALSE)
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
## BURADA ELDE EDILEN DEGERLER TAMSAYI OLMADIGI DURUMDA HATA VERIYOR. BU SEBEPLE OVERALL DEGERLERIN
## KULLANILMASI DAHA UYGUNDUR. ANCAK ELDE EDILEN SONUCLARDAKI P-DEGERLERI VE GUVEN ARALIKLARININ
## DIKKATE ALINMAMASI GEREKIYOR. BU BILGININ BIR NOT OLARAK VERILMESI UYGUN OLABILIR.
tmp <- tmp / model.fit$control$repeats
tmp.attr <- attributes(tmp)
names(tmp.attr$dimnames) <- c("Prediction", "Reference")
attributes(tmp) <- tmp.attr
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
} else if (method == "NBLDA"){
### Calculate train set performances using repeated cross-validation:
folds <- foldIndex(n = nrow(colData(data)), nFolds = control$number, repeats = control$repeats)
parallel <- control$parallel
if (parallel){
nn <- length(folds$indexIn)
fold.tmp <- folds$indexIn
trainResults.AllFolds <- foreach(i = 1:nn, .inorder = FALSE, .multicombine = TRUE,
.export = c("NullModel", "NullModelTest", "GetDnb", "Soft",
"trainNBLDA", "x", "y", "fold.tmp", "type")) %dopar% {
idx <- fold.tmp[[i]]
input.foldIn <- x[idx, ]
output.foldIn <- y[idx]
# Samples for validation in this fold.
input.foldOut <- x[-idx, ]
output.foldOut <- y[-idx]
trainResults.fold <- trainNBLDA(x = input.foldIn, y = output.foldIn, xte = input.foldOut, type = type)
### Predictions for train set:
pred.fold <- factor(trainResults.fold$ytehat, levels = levels(y))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
}
names(trainResults.AllFolds) <- names(folds$indexIn)
} else {
trainResults.AllFolds <- lapply(folds$indexIn, function(idx){
input.foldIn <- x[idx, ]
output.foldIn <- y[idx]
# Samples for validation in this fold.
input.foldOut <- x[-idx, ]
output.foldOut <- y[-idx]
trainResults.fold <- trainNBLDA(x = input.foldIn, y = output.foldIn, xte = input.foldOut, type = type)
### Predictions for train set:
pred.fold <- factor(trainResults.fold$ytehat, levels = levels(y))
tbl <- table(Prediction = pred.fold, Reference = output.foldOut)
acc.fold <- sum(diag(tbl))/sum(tbl)
return(list(accuracies = acc.fold, predictions = pred.fold, confTables = tbl))
})
}
acc <- ldply(lapply(trainResults.AllFolds, function(x)x$accuracies), rbind, .id = "Folds")
colnames(acc)[2] <- "Accuracy"
overallAccuracy <- mean(acc[ ,"Accuracy"])
## Final Model
trainedOverall <- trainNBLDA(x = t(counts(data)), y = colData(data)[ ,class.labels], xte = x, type = normalize)
model.fit <- trainedOverall
model.fit[["tuningResults"]] <- list()
model.fit.final <- model.fit
model.fit.final[["overallAccuracy"]] <- overallAccuracy
model.fit.final[["trainParameters"]] <- model.fit$null.out
control$foldIdx <- folds
model.fit[["control"]] <- control
model.fit[["inputs"]] <- list(x = model.fit$x, y = model.fit$y)
model.fit[["foldInfo"]] <- list(foldAccuracies = acc,
foldPredictions = lapply(trainResults.AllFolds, function(x)x$predictions),
foldIndex = folds)
# Confusion matrix over folds and repeats
aggregatedTable <- lapply(trainResults.AllFolds, function(x){
x$confTables
})
tmp <- as.matrix(aggregatedTable[[1]])
for (i in 2:length(aggregatedTable)){
tmp <- tmp + as.matrix(aggregatedTable[[i]])
}
tmp <- tmp / control$repeats
confM <- confusionMatrix(round(tmp, 0), positive = ref)
confM$tableRounded <- round(tmp, 2)
confM$table <- round(tmp, 0)
attr(confM, "class") <- "confMat"
}
# ## discrete.train adı ile bir S4 class yazılacak.
trainedModel <- new("discrete.train",
inputs = model.fit$inputs,
control = model.fit$control,
crossValidatedModel = model.fit,
tuningResults = model.fit$tuningResults,
finalModel = model.fit.final,
callInfo = list(method = method, normalize = normalize,
class.labels = class.labels, class.names = as.character(unique(colData(data)[ ,class.labels])),
ref = ref))
## All the information about classification model.
modelInfo <- new("MLSeqModelInfo",
method = method,
transformation = NA_character_,
normalization = normalize,
preProcessing = NA_character_,
ref = ref,
control = trainedModel@control, ## PLDA'da kullanılan discreteControl(...) objesi
confusionMat = confM, ## Cross-validated confusion matrix
trainedModel = trainedModel,
trainParameters = trainedModel@finalModel$trainParameters,
call = list(call = call, args = arg.list))
if (transform){
transformedData <- model.fit.final$x
} else {
transformedData <- NULL
}
result = new("MLSeq",
modelInfo = modelInfo,
inputObject = list(rawData = x, transformedData = transformedData, conditions = y))
## Metadata for MLSeq object.
meta <- new("MLSeqMetaData", classLabel = class.labels, rawData.DESeqDataSet = data)
result@metaData <- meta
return(result)
}
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