Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • oscarluoinau
    Junior Member
    • Nov 2011
    • 6

    #1

    Cufflinks memory usage

    Hi all,
    I am having trouble with running Cufflinks on PE RNA-Seq libraries generated from HiSeq machine. I have used Tophat to successfully mapped those PE reads (about 160 millions reads), which gave me a BAM file about 6GB for each library. Then I fed the BAM file to Cufflinks running with 20 cores. Now the problem is it seems Cufflinks is taking more than 120GB ram, and is taking very long (about a week) to run one library. Have any of you had similar experience? Am I doing something wrong? Any suggestions? Thanks!
  • Nicolas
    Member
    • Apr 2009
    • 41

    #2
    Which reference annotations are you using? I had similar experience with gencode annotations (>2.5 millions annotations). I then switched to RefSeq annotations and the Cufflinks runs are now much shorter. Of course, it's quantify much less potential transcripts, but for most applications, that can be sufficient.

    Comment

    • jbrwn
      Member
      • Mar 2011
      • 37

      #3
      in addition to posting your reference, you may want to post which options you're utilizing in cufflinks.

      Comment

      • oscarluoinau
        Junior Member
        • Nov 2011
        • 6

        #4
        Right. I am also using the Gencode annotation. I think I will experiment with other annotation file to see how it goes. The options I am utilizing in Cufflinks are simply specifying the reads come from PE reads (i.e. --fr-unstranded).

        Comment

        • kjlee
          Member
          • Jun 2011
          • 12

          #5
          oscar,

          did you ever get an answer or a work around? I am running cufflinks on a similar sized bam file and am also running out of memory.

          cheers,

          Comment

          • oscarluoinau
            Junior Member
            • Nov 2011
            • 6

            #6
            I couldn't get the job done until upgraded to the latest version of Cufflinks which seems to use less memory. Good luck!

            Comment

            • kjlee
              Member
              • Jun 2011
              • 12

              #7
              Hey Oscar,

              I am running the newest version of Cufflinks (I literally downloaded it this week). I got Cufflinks to run on a small sub-set of reads (about 4 million paired end reads, 100nt with ~200nt inner gap). But the whole data-set is ~50X bigger. How many reads did you use? And what (approximately) was the memory usage for your file size (RAM per GB of the bam/sam file)?

              Cheers,

              Comment

              • oscarluoinau
                Junior Member
                • Nov 2011
                • 6

                #8
                Hi,
                I don't remember the exact numbers as it was about a year ago. One thing I do remember is I was lucky enough to utilize a machine with 1TB RAM, and I used about 500GB for about 160 million reads. I hope this helps. Good luck!

                Comment

                • kjlee
                  Member
                  • Jun 2011
                  • 12

                  #9
                  We only have one compute node with that much memory on our cluster and I didn't want to usurp it if I didn't have to. But I guess that's what the resources are for. Thanks Oscar. (Also, about how long did it take to run?)

                  Cheers,

                  Comment

                  • oscarluoinau
                    Junior Member
                    • Nov 2011
                    • 6

                    #10
                    Expect it to run longer than a week.

                    Comment

                    Latest Articles

                    Collapse

                    • SEQadmin2
                      Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                      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
                      ...
                      10-14-2026, 09:55 AM
                    • SEQadmin2
                      New Genomics Technologies Take Aim at Long-Standing Limits
                      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
                      ...
                      09-28-2026, 10:25 AM

                    ad_right_rmr

                    Collapse

                    News

                    Collapse

                    Topics Statistics Last Post
                    Started by SEQadmin2, 10-15-2026, 10:52 AM
                    0 responses
                    25 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 10-14-2026, 05:39 AM
                    0 responses
                    31 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 10-13-2026, 09:56 AM
                    0 responses
                    28 views
                    0 reactions
                    Last Post SEQadmin2  
                    Started by SEQadmin2, 10-09-2026, 11:14 AM
                    0 responses
                    28 views
                    0 reactions
                    Last Post SEQadmin2  
                    Working...