[Bioc-devel] memory inefficiency problem of building MSPC packages
Jurat, Have you tried posting on the bioconductor support site ( support.bioconductor.org)? That is the appropriate venue for usage questions such as yours, and I suspect you may get a better response there. The bioc-devel mailinglist is intended for a different type of question. Best, ~G
On Mon, Aug 1, 2016 at 11:53 PM, Jurat Shayidin <juratbupt at gmail.com> wrote:
Bioc-devel:
I haven been developing Bioconductor Package for multiple sample peak
calling, and all unit test for my packages is done efficiently. However, I
have one minor problem that cause memory inefficiency when building the
packages in my machines. To get straight, I am going to find overlap for
multiple GRanges objects simultaneously and proceed joint analysis for
multiple ChIP-Seq sample to rescue weak enriched region by helping with
co-localized evidence of multiple GRanges . After I reviewed all my source
code, indeed some paired overlap repeated many times that cause unnecessary
memory usage.
This is my custom function that I developed, it works perfectly in my
current workflow, but cause memory inefficiency problem.
grs <- GRangeslist(gr1, gr2, gr3, gr4, ...)
overlap <- function(grs, idx=1L, FUN=which.min) {
chosen <- grs[[idx]]
que.hit <- as(findOverlaps(chosen), "List")
sup.hit <- lapply(grs[-idx], function(ele_) {
ans <- as(findOverlaps(chosen, ele_), "List")
out.idx0 <- as(FUN(extractList(ele_$p.value, ans)), "List")
out.idx0 <- out.idx0[!is.na(out.idx0)]
ans <- ans[out.idx0]
})
res <- c(list(que.hit), sup.hit)
return(res)
}
How can I optimize my custom function without memory inefficiency? How can
I get rid of repeated overlapped paired GRanges? How can I efficiently
solve this issue? Can anyone propose possible ideas to get through this
problem? Thanks a lot
--
Jurat Shahidin
Ph.D. candidate
Dipartimento di Elettronica, Informazione e Bioingegneria
Politecnico di Milano
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