Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • dfhdfh
    Member
    • Jan 2013
    • 46

    #1

    New TopHat version (2.0.7): Uses only one core?

    Hi there,
    I just installed the new TopHat version 2.0.7 along with the new Bowtie 2.0.6. Everything works fine and without errors, except for the fact that it seems to run on only one core. Before this update, I used TopHat 2.0.6 with Bowtie 2.0.4 and -p 8 worked absolutely perfectly. Now with the new version, I use the exact same command, including -p 8, but the runs take forever and the CPU usage shows only 100% CPU usage instead of the expected 800%. Should I downgrade to Bowtie 2.0.5 (as this is the version stated in the news post of TopHat 2.0.7) or is this a bug? Does anyone else have this problem?

    Jens

    Edit: The complete command I'm using is the following:

    tophat -r 50 --mate-std-dev 30 -p 8 --no-coverage-search --microexon-search --library-type fr-unstranded
    Last edited by dfhdfh; 01-30-2013, 01:39 AM.
  • Jetse
    Member
    • Nov 2012
    • 38

    #2
    Not each step is multithreaded in tophat, did you check multiple times during different steps of the process?

    Comment

    • dfhdfh
      Member
      • Jan 2013
      • 46

      #3
      Yeah, I did. During the mapping it should be at 800%.
      I downgraded to Bowtie 2.0.5 and now it shows a CPU usage of 800% at the mapping steps but it is unbelievably slow. The same run with the same options takes about 5-7x the time it did with TopHat 2.0.6/Bowtie 2.0.4. How can this be?

      Comment

      • benjamir
        Junior Member
        • Nov 2012
        • 4

        #4
        dfhdfh,
        Tophat 2.0.7 is the first version of the program I have ever used. I am also using Bowtie 2.0.6. My initial test run of Tophat has entered its fourth day.

        The test is paired-end ( ~100bp qual trimmed x 2, 36.6E6 reads) with options that “may greatly increase mapping accuracy”, mapping every read to transcriptome, genome, and splice variants:
        tophat -p 8 --library-type fr-unstranded --read-realign-edit-dist 0 --min-anchor-length 6 --microexon-search -G

        One person in my lab suggested the long run could be due to the microexon search option. It seems in your case, this has been ruled out.

        Comment

        • dfhdfh
          Member
          • Jan 2013
          • 46

          #5
          It is really weird, indeed. I had some trouble with 2.0.6 (broken gzip pipe, CIGAR errors, quality and sequence inconsistent) that seem to be gone with the new version. Before, I always deleted the "faulty" reads (which were not faulty if you looked at them) and it then ran through or produced another error. With 2.0.7, these problems are gone, which is why I would like to use it as my daily solution from here on out. It seems that I have to live with it taking a lot more time than the previous version, though

          Comment

          • vpr8
            Junior Member
            • Nov 2012
            • 1

            #6
            I also have bowtie 2.0.6 and TopHat 2.0.6 and it's also only using one core during mapping

            Comment

            • yzzhang
              Member
              • Jan 2013
              • 67

              #7
              I used tophat 2.0.7 with bowtie 2.0.6 it works well. for my 50 million *2 reads, it usually costs 9 hours when I use 12 cpus

              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
              26 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              32 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-13-2026, 09:56 AM
              0 responses
              29 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...