The patched version is working more than twice as fast (actually went just a little bit faster but using -p16 instead of -p32), so that's good.
But now I'm having a problem that I've encountered with other Tuxedo tools (cuffquant and cuffdiff) with both patched and unpatched 2.2.1, I'm getting a segfault even though I'm not running of of memory. In this case I used patched Cufflinks 2.2.1 on two different .bam files and got a segfault for both files at the same locus near the beginning of "Re-estimating abundances with bias and multi-read correction". I don't have an overabundance of reads at or near this location when I visualize the aligned files. But I don't think it's an issue with a specific locus since in cuffdiff I tried masking the offending locus then it just segfaulted somewhere else, in both cases near the beginning of "Testing for differential expression and regulation in locus".
Unconfigured Ad
Collapse
X
-
Actually I just came across this and I'm currently trying it, if that is the cause of my problem do you know if I should expect a large or small speed improvement using this patch?Originally posted by offspring View PostOne "long runtime" problem in cufflinks 2.2.1 related to an inefficient data structure has been reported and fixed recently: https://groups.google.com/forum/#!to...rs/UzLCJhj3lUE
It will be part of cufflinks 2.2.2 (not released yet), would be interesting to know if this fixes your issue.
The commit in question: https://github.com/cole-trapnell-lab...a0292d507f17b6
ChrisLast edited by biocomputer; 01-07-2015, 02:43 PM.
Leave a comment:
-
One "long runtime" problem in cufflinks 2.2.1 related to an inefficient data structure has been reported and fixed recently: https://groups.google.com/forum/#!to...rs/UzLCJhj3lUE
It will be part of cufflinks 2.2.2 (not released yet), would be interesting to know if this fixes your issue.
The commit in question: https://github.com/cole-trapnell-lab...a0292d507f17b6
Chris
Leave a comment:
-
Thank you, yes I definitely plan to try other programs besides cufflinks/Tuxedo to compare results.
Leave a comment:
-
I have not used Cufflinks several years, but last time I used it, I was analyzing human liver samples and had to remove all albumin-mapped reads to prevent it from hanging. I recommend against it; it's just not very reliable or predictable - it was faster for me to write my own aligner and analysis toolchain than to wait for the Tuxedo pipeline to finish.Originally posted by biocomputer View PostCufflinks 2.2.1 is taking a really long time. I start with 45 million 100bp paired-end, rRNA depleted, stranded reads aligned with STAR, 24 million uniquely align, 15 million are multimappers, using a sorted .bam as the input for cufflinks. Cufflinks command is:
Things to note:Code:cufflinks -o outputFolder -p 32 -g gencode.v2.annotation.gtf -M maskFile.gtf -b mm10.fa -u --library-type fr-secondstrand inputSorted.bam
-p 32, all 32 CPU's are in use for pretty much the entire time, here's the usage for the past 24 hours from the 32-CPU node I've been using, you can see it going down as threads are completing at the end of the cufflinks run.
The mask file is masking out a few very highly expressed genes which make up almost 20% of all reads. When I didn't mask these out it got hung up at these loci.
The library type is reversed because I'm following these instructions.
After 3.5 days I think it's just about done (it's at "waiting for 18 threads to complete"). Given that the number of input reads isn't huge (especially once all the masked reads are accounted for) and I'm using 32 CPU's, I'm surprised it's taking so long. It doesn't seem like it's getting hung up at any specific spots, but it does seem to slow down as it goes, until it's taking many hours for each of the last few percent.
Is this runtime normal? Anything I can do to speed it up?
Currently, DESeq seems to be a better choice than Cufflinks.
Leave a comment:
-
Cufflinks runtime
Cufflinks 2.2.1 is taking a really long time. I start with 45 million 100bp paired-end, rRNA depleted, stranded reads aligned with STAR, 24 million uniquely align, 15 million are multimappers, using a sorted .bam as the input for cufflinks. Cufflinks command is:
Things to note:Code:cufflinks -o outputFolder -p 32 -g gencode.v2.annotation.gtf -M maskFile.gtf -b mm10.fa -u --library-type fr-secondstrand inputSorted.bam
-p 32, all 32 CPU's are in use for pretty much the entire time, here's the usage for the past 24 hours from the 32-CPU node I've been using, you can see it going down as threads are completing at the end of the cufflinks run.
The mask file is masking out a few very highly expressed genes which make up almost 20% of all reads. When I didn't mask these out it got hung up at these loci.
The library type is reversed because I'm following these instructions.
After 3.5 days I think it's just about done (it's at "waiting for 18 threads to complete"). Given that the number of input reads isn't huge (especially once all the masked reads are accounted for) and I'm using 32 CPU's, I'm surprised it's taking so long. It doesn't seem like it's getting hung up at any specific spots, but it does seem to slow down as it goes, until it's taking many hours for each of the last few percent.
Is this runtime normal? Anything I can do to speed it up?
Latest Articles
Collapse
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
-
by SEQadmin2
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...-
Channel: Articles
-
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Yesterday, 11:13 AM
|
0 responses
19 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 11:13 AM
|
||
|
Started by SEQadmin2, Yesterday, 10:48 AM
|
0 responses
18 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 10:48 AM
|
||
|
Started by SEQadmin2, 10-15-2026, 10:52 AM
|
0 responses
36 views
0 reactions
|
Last Post
by SEQadmin2
10-15-2026, 10:52 AM
|
||
|
Started by SEQadmin2, 10-14-2026, 05:39 AM
|
0 responses
42 views
0 reactions
|
Last Post
by SEQadmin2
10-14-2026, 05:39 AM
|
Leave a comment: