library("SVM2CRMdata")
library("GenomicRanges")
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)
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)
data_enhancer_svm<-createSVMinput(inputpos=table.final.overlap,inputfull=completeTABLE,label1="enhancers",label2="not_enhancers")
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