I posted the question on the support website of bioconductor and found a solution for the problem. Here's the link for it:
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Here's my sessionInfo(). Does it look right?
R version 3.1.2 (2014-10-31)
Platform: x86_64-apple-darwin13.4.0 (64-bit)
locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
attached base packages:
[1] stats4 parallel stats graphics grDevices utils datasets methods base
other attached packages:
[1] GenomicAlignments_1.2.0 Rsamtools_1.18.1 Biostrings_2.34.0 XVector_0.6.0
[5] GenomicRanges_1.18.3 GenomeInfoDb_1.2.2 IRanges_2.0.0 S4Vectors_0.4.0
[9] BiocGenerics_0.12.0 BiocInstaller_1.16.1
loaded via a namespace (and not attached):
[1] base64enc_0.1-2 BatchJobs_1.5 BBmisc_1.8 BiocParallel_1.0.0 bitops_1.0-6
[6] brew_1.0-6 checkmate_1.5.0 codetools_0.2-9 DBI_0.3.1 digest_0.6.4
[11] fail_1.2 foreach_1.4.2 iterators_1.0.7 RSQLite_1.0.0 sendmailR_1.2-1
[16] stringr_0.6.2 tools_3.1.2 zlibbioc_1.12.0
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Thank you for your reply. I am using the latest R version. I am not sure what's the difference between the two links you provided above. They both seem to link to the same downloadable links:
source("http://bioconductor.org/biocLite.R")
biocLite("GenomicAlignments")
Is there a way to have a link to the R-devel version so i could try it? I even tried running the same thing over 30 hours. It looked like it was consuming memory (~600 megabyte ram) but it still took 30 hours without any results.
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Habbas
are you using the most recent versions of R and the packages?
See http://www.bioconductor.org/packages...lignments.html (version 1.2.1) and in fact I would even try R-devel and http://www.bioconductor.org/packages...lignments.html (version 1.3.19).
If the problem persists, I recommend contacting the maintainer of the "GenomicAlignments" package (which contains summarizeOverlaps) directly, possibly via the Bioconductor forum.
Kind regards
Wolfgang
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summarizeOverlaps too, too slow then freeze
I hope someone can help in this issue.
I have 8 bam files from mm9 alignment, each ~4-5 geg in size. When I run summarizeOverlaps over 3 files, it takes 2-3 hours to finish and it works although my computer almost freezes up. But when I put the 8 files together, then keep it on overnight (as it takes too long to wait), the computer freezes (although it is 16 geg i7 mac, so supposed to be powerful) and the command never results in anything.
I am making my own txdb file from gtf that I used for the alignment to match the naming of the chromosomes. (script is below).
Do you have any tips on how I can get the summzerOverlaps to work on the 8 files to create one se file without freezing up the computer? I have been trying to do that for the past 2 week and always same result.
Any input is appreciated.
here’s the script:
library("DESeq2")
library("GenomicFeatures")
library("Rsamtools")
library("GenomicAlignments")
library("GenomicRanges”)
mm9_from_cluster_gtf_txdb <- makeTranscriptDbFromGFF(file="~/Desktop/genes.gtf", format="gtf”)
head(seqlevels(mm9_from_cluster_gtf_txdb))
saveDb(mm9_from_cluster_gtf_txdb, file="/Path/To/Libraries/TxDB/mm9_from_cluster_Ensembl_txdb.sqlite”)
exonsByGene<-exonsBy(mm9_from_cluster_gtf_txdb,by="gene")
seqinfo(exonsByGene)
fls <- list.files("/Path/To/BamFiles", pattern="paired.accepted_hits.bam", full= TRUE)
fls
Experiment <- c(fls[2:8], fls[1])
Experiment
bamLst_experiment <- BamFileList(Experiment, yieldSize=100000)
seqinfo(bamLst_experiment)
se_test_experiment <- summarizeOverlaps(exonsByGene,bamLst_experiment, mode="Union", singleEnd=FALSE, ignore.strand=TRUE, fragments=TRUE) <<<This is the step that freezes the computer when I run the 8 of the files together.Last edited by habbas; 12-29-2014, 02:37 PM.
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