Seqanswers Leaderboard Ad

Collapse

Announcement

Collapse
No announcement yet.
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

  • Error in Trinity - Chrysalis: ReadsToTranscripts

    Hello,

    I am running trinity to perform some de novo assemblies and everything was doing ok. Now I am facing a really weird problem that is making the trinity die everytime.

    Processing reads:
    reading another 10000000... done. Read 5427877 reads.

    libgomp: Out of memory allocating 1456 bytes
    COMMAND: /home/user/oliveira/Assemblers/trinityrnaseq_r20131110/Chrysalis/ReadsToTranscripts -i both.fa -f /scratch/trinity_test_4a/chrysalis/bundled_iworm_contigs.fasta -t 1 -o /scratch/trinity_test_4a/chrysalis -max_mem_reads 10000000
    Died with exit code 256
    That is the problem, and it is quite weird because it looks like it is a memory problem, but I already performed some assemblies with bigger datasets and this problem never happened. Someone knows what is happening? Someone already faced this same problem? I will really appreciate some help, because I have no idea how to solve this.

    Best regards,
    André
    Last edited by aloliveira; 02-02-2014, 03:19 AM. Reason: Problem solved.

  • #2
    More informations about the error.

    COMMAND: /home/user/oliveira/Assemblers/trinityrnaseq_r20131110/Chrysalis/ReadsToTranscripts -i both.fa -f /scratch/trinity_test_4a/chrysalis/bundled_iworm_contigs.fasta -t 8 -o /scratch/trinity_test_4a/chrysalis -max_mem_reads 10000000
    Died with exit code 256
    Exiting.
    core file size (blocks, -c) 0
    data seg size (kbytes, -d) unlimited
    scheduling priority (-e) 0
    file size (blocks, -f) unlimited
    pending signals (-i) 386252
    max locked memory (kbytes, -l) 64
    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) 8192
    cpu time (seconds, -t) unlimited
    max user processes (-u) 1024
    virtual memory (kbytes, -v) unlimited
    file locks (-x) unlimited

    Error, the Chrysalis process failed:
    Error, cmd: /home/user/oliveira/Assemblers/trinityrnaseq_r20131110/Chrysalis/Chrysalis -i both.fa -iworm /scratch/trinity_test_4a/inchworm.K25.L25.DS.fa -o /scratch/trinity_test_4a/chrysalis -cpu 8 -min_glue 2 -min_iso_ratio 0.05 -glue_factor 0.05 -weldmer_size 48 -min 200 -dist 500 -max_reads 200000 -sort_buffer_size 48G -max_mem_reads 10000000 -paired -reads_for_pairs both.fa -butterfly /home/user/oliveira/Assemblers/trinityrnaseq_r20131110/Butterfly/Butterfly.jar 2>&1 died with ret 65280 at ./Trinity.pl line 1793.

    at ./Trinity.pl line 1322.
    main::run_chrysalis('/scratch/trinity_test_4a/inchworm.K25.L25.DS.fa', 'both.fa', 200, 500, undef, 'both.fa') called at ./Trinity.pl line 1136

    Comment


    • #3
      So, I just solved the problem changing the chrysalis parameter -max_mem_reads to a lower value.

      Comment

      Latest Articles

      Collapse

      • seqadmin
        Essential Discoveries and Tools in Epitranscriptomics
        by seqadmin




        The field of epigenetics has traditionally concentrated more on DNA and how changes like methylation and phosphorylation of histones impact gene expression and regulation. However, our increased understanding of RNA modifications and their importance in cellular processes has led to a rise in epitranscriptomics research. “Epitranscriptomics brings together the concepts of epigenetics and gene expression,” explained Adrien Leger, PhD, Principal Research Scientist...
        04-22-2024, 07:01 AM
      • seqadmin
        Current Approaches to Protein Sequencing
        by seqadmin


        Proteins are often described as the workhorses of the cell, and identifying their sequences is key to understanding their role in biological processes and disease. Currently, the most common technique used to determine protein sequences is mass spectrometry. While still a valuable tool, mass spectrometry faces several limitations and requires a highly experienced scientist familiar with the equipment to operate it. Additionally, other proteomic methods, like affinity assays, are constrained...
        04-04-2024, 04:25 PM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 04-11-2024, 12:08 PM
      0 responses
      59 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 10:19 PM
      0 responses
      57 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-10-2024, 09:21 AM
      0 responses
      53 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 04-04-2024, 09:00 AM
      0 responses
      56 views
      0 likes
      Last Post seqadmin  
      Working...
      X