Description Usage Arguments Details Value Author(s) See Also Examples
This function use a contingency table and then estimate: sensitivity, false positive rate, accurancy, specificity, precision, positive predicted values, negative predicted values, false discovery rates, f-score. Useful to estimate the performance of a model. Internal function of plotROC.
1 | performanceSVM(res)
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res |
a confusion matrix |
Some detailled description
A data.frame with tpr.sensitivity, fpr, acc, spc.specificity, precision, ppv, npv, fdr, fscore.
Guidantonio Malagoli Tagliazucchi guidantonio.malagolitagliazucchi@unimore.it
cisREfind, tuniningParametersCOmbROC, predictionGW
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 | library("GenomicRanges")
library("SVM2CRMdata")
setwd(system.file("data",package="SVM2CRMdata"))
load("CD4_matrixInputSVMbin100window1000.rda")
completeTABLE<-CD4_matrixInputSVMbin100window1000
new.strings<-gsub(x=colnames(completeTABLE[,c(6:ncol(completeTABLE))]),pattern="CD4.",replacement="")
new.strings<-gsub(new.strings,pattern=".norm.w100.bed",replacement="")
colnames(completeTABLE)[c(6:ncol(completeTABLE))]<-new.strings
#list_file<-grep(dir(),pattern=".sort.txt",value=TRUE)
#train_positive<-getSignal(list_file,chr="chr1",reference="p300.distal.fromTSS.txt",win.size=500,bin.size=100,label1="enhancers")
#train_negative<-getSignal(list_file,chr="chr1",reference="random.region.hg18.nop300.txt",win.size=500,bin.size=100,label1="not_enhancers")
setwd(system.file("data",package="SVM2CRMdata"))
load("train_positive.rda")
load("train_negative.rda")
training_set<-rbind(train_positive,train_negative)
#the colnames of the training set should be the same of data_enhancer_svm
colnames(training_set)[c(5:ncol(training_set))]<-gsub(x=gsub(x=colnames(training_set[,c(5:ncol(training_set))]),pattern="sort.txt.",replacement=""),pattern="CD4.",replacement="")
setwd(system.file("extdata", package = "SVM2CRMdata"))
data_level2 <- read.table(file = "GSM393946.distal.p300fromTSS.txt",sep = "\t", stringsAsFactors = FALSE)
data_level2<-data_level2[data_level2[,1]=="chr1",]
DB <- data_level2[, c(1:3)]
colnames(DB)<-c("chromosome","start","end")
label <- "p300"
table.final.overlap<-findFeatureOverlap(query=completeTABLE,subject=DB,select="all")
data_enhancer_svm<-createSVMinput(inputpos=table.final.overlap,inputfull=completeTABLE,label1="enhancers",label2="not_enhancers")
colnames(data_enhancer_svm)[c(5:ncol(data_enhancer_svm))]<-gsub(gsub(x=colnames(data_enhancer_svm[,c(5:ncol(data_enhancer_svm))]),pattern="CD4.",replacement=""),pattern=".norm.w100.bed",replacement="")
listcolnames<-c("H2AK5ac","H2AK9ac","H3K23ac","H3K27ac","H3K27me3","H3K4me1","H3K4me3")
dftotann<-smoothInputFS(train_positive[,c(6:ncol(train_positive))],listcolnames,k=20)
results<-featSelectionWithKmeans(dftotann,5)
resultsFS<-results[[7]]
resultsFSfilter<-resultsFS[which(resultsFS[,2]>median(resultsFS[,2])),]
resultsFSfilterICRR<-resultsFSfilter[which(resultsFSfilter[,3]<0.50),]
listHM<-resultsFSfilterICRR[,1]
listHM<-gsub(gsub(listHM,pattern="_.",replacement=""),pattern="CD4.",replacement="")
selectFeature<-grep(x=colnames(training_set[,c(6:ncol(training_set))]),pattern=paste(listHM,collapse="|"),value=TRUE)
colSelect<-c("chromosome","start","end","label",selectFeature)
training_set<-training_set[,colSelect]
vecS <- c(2:length(listHM))
typeSVM <- c(0, 6, 7)[1]
costV <- c(0.001, 0.01, 0.1, 1, 10, 100, 1000)[6]
wlabel <- c("not_enhancer", "enhancer")
infofile<-data.frame(a=c(paste(listHM,"signal",sep=".")))
infofile[,1]<-gsub(gsub(x=infofile[,1],pattern="CD4.",replacement=""),pattern=".sort.bed",replacement="")
tuningTAB <- tuningParametersCombROC(training_set = training_set, typeSVM = typeSVM, costV = costV,different.weight="TRUE", vecS = vecS[1],pcClass=100,ncClass=400,infofile)
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