Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • angerusso
    Member
    • Oct 2011
    • 47

    #1

    memory error: tophat-fusion-post

    I have ~400 samples where I ran tophat2 fusion. Now I am trying to run tophat-fusion-post which gives the following error:

    Traceback (most recent call last):
    File "/x86_64/tophat/v2.0.8/tophat-fusion-post", line 2627, in <module>
    sys.exit(main())
    File "/x86_64/tophat/v2.0.8/tophat-fusion-post", line 2604, in main
    read_dist(params)
    File "/x86_64/tophat/v2.0.8/tophat-fusion-post", line 1196, in read_dist
    parallel_work(pids, work)
    File "/x86_64/tophat/v2.0.8/tophat-fusion-post", line 731, in parallel_work
    child_id = os.fork()
    OSError: [Errno 12] Cannot allocate memory
    Sat Jun 8 23:50:10 EDT 2013

    Can anyone help me this error? Thanks so much.
  • rnastar
    Member
    • Aug 2013
    • 13

    #2
    I am also have a similar problem. I am wondering if I am not specifying enough memory per parallel job on our cluster (currently 5G)? Any help would be appreciated here.

    Code:
    [2013-12-18 03:44:13] Mapping right_kept_reads.m2g_um_seg1 to genome genome with Bowtie2 (1/2)
    [2013-12-18 03:52:29] Mapping right_kept_reads.m2g_um_seg2 to genome genome with Bowtie2 (2/2)
    [2013-12-18 04:05:24] Searching for junctions via segment mapping
    [2013-12-18 05:27:58] Retrieving sequences for splices
    [2013-12-18 05:37:53] Indexing splices
    Traceback (most recent call last):
      File "./tophat", line 4072, in <module>
        sys.exit(main())
      File "./tophat", line 4038, in main
        user_supplied_deletions)
      File "./tophat", line 3692, in spliced_alignment
        if reads == None or not nonzeroFile(reads):
      File "./tophat", line 1155, in nonzeroFile
        samtools_view = subprocess.Popen(samtools_view_cmd, stdout=subprocess.PIPE)
      File "/usr/local/lib/python2.7/subprocess.py", line 672, in __init__
        errread, errwrite)
      File "/usr/local/lib/python2.7/subprocess.py", line 1111, in _execute_child
        self.pid = os.fork()
    OSError: [Errno 12] Cannot allocate memory

    Comment

    • dfornika
      Junior Member
      • Aug 2009
      • 4

      #3
      I've just run an analysis on ~30 libraries and got a similar error. I was running it on a multi-user machine with ~60 GB of RAM.

      Code:
      Traceback (most recent call last):
        File "/home/dfornika/bin/tophat-2.0.12/tophat-fusion-post", line 2644, in <module>
          sys.exit(main())
        File "/home/dfornika/bin/tophat-2.0.12/tophat-fusion-post", line 2621, in main
          read_dist(params)
        File "/home/dfornika/bin/tophat-2.0.12/tophat-fusion-post", line 1206, in read_dist
          parallel_work(pids, work)
        File "/home/dfornika/bin/tophat-2.0.12/tophat-fusion-post", line 737, in parallel_work
          child_id = os.fork()
      OSError: [Errno 12] Cannot allocate memory
      I did monitor the processes somewhat using 'top' and they seemed to be using ~20% of available RAM. I'm not sure what the actual limitation is that we're running into.

      It seems like tophat-fusion-post is designed to be run on a large(ish) group of samples at once. Is there any sensible way to break a large multi-sample analysis down into smaller groups? Is that likely to solve this memory issue?

      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, 10-22-2026, 11:13 AM
      0 responses
      35 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-22-2026, 10:48 AM
      0 responses
      25 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-15-2026, 10:52 AM
      0 responses
      41 views
      0 reactions
      Last Post SEQadmin2  
      Started by SEQadmin2, 10-14-2026, 05:39 AM
      0 responses
      45 views
      0 reactions
      Last Post SEQadmin2  
      Working...