Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • ECHo
    Member
    • Jan 2010
    • 17

    #1

    trinity error

    Trinity is the new de novo transcriptome assembly software, and I'm interested in the the software.
    According to the manual listed on the website, I tried to test it.
    However, there are some errors as follows:
    COMMAND: /opt/trinityrnaseq_r2011-08-20/Chrysalis/GraphFromFasta -i inchworm.K25.L48.DS.fa -r both.fa > chrysalis/components.out
    Died with exit code 35072
    Exiting.
    Error, chrysalis did not report butterfly commands file: /data/echo/SRAdb/trinity_out_dir/chrysalis/butterfly_commands at /opt/trinityrnaseq_r2011-08-20/Trinity.pl line 396
    main::run_chrysalis('inchworm.K25.L48.DS.fa', 'both.fa', 200, 300, 'undef') called at /opt/trinityrnaseq_r2011-08-20/Trinity.pl line 317
    Error, the Chrysalis process failed:
    Error, cmd: /opt/trinityrnaseq_r2011-08-20/Chrysalis/Chrysalis -i both.fa -iworm inchworm.K25.L48.DS.fa -o chrysalis -min 200 -dist 300 -butterfly /opt/trinityrnaseq_r2011-08-20/Butterfly/Butterfly.jar died with ret 65280 at /opt/trinityrnaseq_r2011-08-20/Trinity.pl line 571.

    In nearly all cases, this is related to not having the stacksize set to unlimited, a prerequisite to running Trinity.
    Please visit:

    http://trinityrnaseq.sourceforge.net...aq.html#ques_E

    for details.

    I couldn't understand since my settings for the stack size is unlimited:
    core file size (blocks, -c) 0
    data seg size (kbytes, -d) unlimited
    scheduling priority (-e) 0
    file size (blocks, -f) unlimited
    pending signals (-i) 335872
    max locked memory (kbytes, -l) 32
    max memory size (kbytes, -m) unlimited
    open files (-n) 1024
    pipe size (512 bytes, -p) 8
    POSIX message queues (bytes, -q) 819200
    real-time priority (-r) 0
    stack size (kbytes, -s) unlimited
    cpu time (seconds, -t) unlimited
    max user processes (-u) 335872
    virtual memory (kbytes, -v) unlimited
    file locks (-x) unlimited

    How could I do?
    Could somebody give a hint?
    Thanks a lot.
  • avian
    Junior Member
    • Aug 2011
    • 1

    #2
    You may wish to post this question to the Trinity mailing list for a better explanation of what might have gone wrong, but another common issue relates to the amount of RAM trinity requires. Do you have sufficient resources for the number of reads you are using?

    Comment

    • tboothby
      Member
      • May 2011
      • 56

      #3
      I am having a similar problem. My stacksize is set to unlimited. My input is 78M and I have 96G of RAM (Trinity website suggests 1G for every 1M). Has anybody with this problem found a fix?

      Comment

      • westerman
        Rick Westerman
        • Jun 2008
        • 1104

        #4
        You could try, as an experiment, running with half of your sequences in order to see if there is a problem with memory or if there is something else wrong.

        I agree with the suggestion of sending to the Trinity mailing list. Brian Haas -- one of the Trinity authors -- is very helpful.

        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
          ...
          Yesterday, 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, Yesterday, 05:39 AM
        0 responses
        11 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-13-2026, 09:56 AM
        0 responses
        14 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 10-09-2026, 11:14 AM
        0 responses
        27 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 09-29-2026, 09:51 AM
        0 responses
        77 views
        0 reactions
        Last Post SEQadmin2  
        Working...