Nothing
library(Biobase)
if(file.exists("ovarian_esets.rda")){
load("ovarian_esets.rda")
}else{
library(curatedOvarianData)
library(logging)
source(system.file("extdata",
"patientselection_all.config",package="curatedOvarianData"))
min.number.of.genes <- 2000
source(system.file("extdata", "createEsetList.R", package =
"curatedOvarianData"))
rm(list=ls(pattern="_eset"))
save(esets, file="ovarian_esets.rda")
}
esets <- esets[c("GSE14764_eset", "GSE2109_eset", "GSE32062.GPL6480_eset")]
table(table(unlist(lapply(esets, sampleNames))))
library(doppelgangR)
res.orig <- doppelgangR(esets, phenoFinder.args=NULL, smokingGunFinder.args=NULL, within.datasets.only=TRUE)
confirmed.dups <- summary(res.orig)[-7, 1:2]
dups <- c(confirmed.dups[, 1], confirmed.dups[, 2])
dups <- sub(".+:", "", dups)
reduceEset <- function(eset, dups, n){
keeps <- which(sampleNames(eset) %in% dups)
maybes <- which(!sampleNames(eset) %in% dups)
n.extras <- n - length(keeps)
keeps <- c(keeps, sample(maybes, n.extras))
return(eset[, keeps])
}
if(file.exists("ovc_small_datasets.rds")){
res <- readRDS("ovc_small_datasets.rds")
}else{
res <- list()
for (i in 1:length(esets)){
res[[i]] <- list()
nseq <- c(5, seq(10, ncol(esets[[i]]), by=10))
min.keeps <- sum(sampleNames(esets[[i]]) %in% dups)
nseq <- nseq[nseq > min.keeps]
for (k in 1:length(nseq)){
eset <- reduceEset(esets[[i]], dups, nseq[k])
res[[i]][[k]] <- doppelgangR(eset, phenoFinder.args=NULL, smokingGunFinder.args=NULL, intermediate.pruning=FALSE)
}
names(res[[i]]) <- nseq
}
names(res) <- names(esets)
saveRDS(res, file="ovc_small_datasets.rds")
}
for (i in 1:length(res)){
print(" ")
print(names(res)[i])
print(sapply(res[[i]], function(x) nrow(summary(x))))
}
plot(res[["GSE32062.GPL6480_eset"]][[1]])
plot(res[["GSE32062.GPL6480_eset"]][[2]])
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