Header Leaderboard Ad

Collapse

fastq_to_fasta segmentation fault (core dumped)

Collapse

Announcement

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

  • fastq_to_fasta segmentation fault (core dumped)

    Hi, I am trying to convert my fastq files which have been stitched using multiple_join_paired_ends.py under qiime-1.9.1
    Now my fastq joined files look okay, but when I try to convert them to fasta I am having trouble. for a single file test I get the error
    Code:
    less fastq2fasta.single.file.sh.e378704
    
    /var/spool/sge_prod/hb01s2b15/job_scripts/378704: line 7: 26760 Segmentation fault      (core dumped) fastq_to_fasta -i RIFSAMPLEA_S1.join.fastq -o RIFSAMPLEA_S1.join.fasta
    fastq2fasta.single.file.sh.e378704 (END)

    This is the job script that I used.

    Code:
    less fastq2fasta.single.file.sh
    
    #$ -l h_rt=24:00:00
    #$ -cwd
    #$ -V
    #$ -l h_vmem=8G
    #$ -M [email protected]
    
     fastq_to_fasta -i RIFSAMPLEA_S1.join.fastq -o RIFSAMPLEA_S1.join.fasta
    
    
    fastq2fasta.single.file.sh (END)
    I have looked at the log for the job so I can see that it fails as it is setting up and probably fails at the very beginning of that. Also the log indicates that no memory has been used. I heard, that a segmentation fault is often a problem with allocating memory but it normally occurs late on in the execution of a program when nearly all of the memory has been used and the programm asks for more memory than there is left. But this is definitely not a case here.

    Can anybody please help me how to fix this problem?
    Thanks,
    Mitra

  • #2
    First thing I'd try is throwing a ton of memory at it. See if it runs with 64G of memory. If it does maybe slim it down for other jobs. Segmentation faults say to me that the problem has something to do with memory allocation and not necessarily the task itself. I know that you know that, and so suspect that there is something else going on, but even still, I would keep digging into the memory issue as being the problem for a long while. Permissions and memory. Good luck!

    Comment


    • #3
      Fastq to fasta should not require much memory. Try BBMap's reformat.sh:

      Code:
      reformat.sh in=file.fastq out=file.fasta -Xmx1g

      Comment

      Latest Articles

      Collapse

      • seqadmin
        How RNA-Seq is Transforming Cancer Studies
        by seqadmin



        Cancer research has been transformed through numerous molecular techniques, with RNA sequencing (RNA-seq) playing a crucial role in understanding the complexity of the disease. Maša Ivin, Ph.D., Scientific Writer at Lexogen, and Yvonne Goepel Ph.D., Product Manager at Lexogen, remarked that “The high-throughput nature of RNA-seq allows for rapid profiling and deep exploration of the transcriptome.” They emphasized its indispensable role in cancer research, aiding in biomarker...
        09-07-2023, 11:15 PM
      • seqadmin
        Methods for Investigating the Transcriptome
        by seqadmin




        Ribonucleic acid (RNA) represents a range of diverse molecules that play a crucial role in many cellular processes. From serving as a protein template to regulating genes, the complex processes involving RNA make it a focal point of study for many scientists. This article will spotlight various methods scientists have developed to investigate different RNA subtypes and the broader transcriptome.

        Whole Transcriptome RNA-seq
        Whole transcriptome sequencing...
        08-31-2023, 11:07 AM

      ad_right_rmr

      Collapse

      News

      Collapse

      Topics Statistics Last Post
      Started by seqadmin, 09-22-2023, 09:05 AM
      0 responses
      14 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 09-21-2023, 06:18 AM
      0 responses
      12 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 09-20-2023, 09:17 AM
      0 responses
      13 views
      0 likes
      Last Post seqadmin  
      Started by seqadmin, 09-19-2023, 09:23 AM
      0 responses
      28 views
      0 likes
      Last Post seqadmin  
      Working...
      X