Nothing
pipeline.genesetStatisticSamples <- function()
{
### perform GS analysis ###
t.ensID.m <<- t.g.m[which(rownames(indata) %in% names(gene.info$ids)),]
t.ensID.m <<- do.call(rbind, by(t.ensID.m, gene.info$ids, colMeans))
if (preferences$activated.modules$geneset.analysis.exact)
{
gs.null.list <- list()
for (i in seq_along(gs.def.list))
{
gs.null.list[[i]] <-
list(Genes=sample(unique.protein.ids, length(gs.def.list[[i]]$Genes)))
}
null.scores <- sapply( 1:ncol(indata), function(m)
{
all.gene.statistic <- t.ensID.m[,m]
spot.gene.ids <- unique.protein.ids
scores <- GeneSet.GSZ(spot.gene.ids, all.gene.statistic, gs.null.list)
return(scores)
})
null.culdensity <- ecdf(abs(unlist(null.scores)))
}
spot.list.samples <<- lapply(seq_along(spot.list.samples) , function(m)
{
x <- spot.list.samples[[m]]
all.gene.statistic <- t.ensID.m[,m]
spot.gene.ids <- unique.protein.ids
x$GSZ.score <-
GeneSet.GSZ(spot.gene.ids, all.gene.statistic, gs.def.list, sort=FALSE)
# GeneSet.maxmean(all.gene.statistic, gs.def.list)
if (preferences$activated.modules$geneset.analysis.exact)
{
x$GSZ.p.value <- 1 - null.culdensity(abs(x$GSZ.score))
names(x$GSZ.p.value) <- names(x$GSZ.score)
}
return(x)
})
names(spot.list.samples) <<- colnames(indata)
### GSZ table output ###
samples.GSZ.scores <<- do.call(cbind, lapply(spot.list.samples, function(x)
{
return(x$GSZ.score[names(gs.def.list)])
}))
}
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