Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Robo
    Junior Member
    • Jan 2020
    • 3

    #1

    FastQC problems

    Greetings to every one. Here we have another newbie who made the reckless decision to throw himself in bioinformatics . I was given certain sequences from nanopore and pacbio, so really long sequences. Managed the program to work correctly in the server as a perl script but when I run it with the data as an argument I get the following error

    Exception in thread "Thread-1" java. lang. Out Of Memory Error: Java heap space
    at uk.ac.babraham.FastQC.Utilities.QualityCount.<init>(QualityCount.java:33)
    at
    uk.ac.babraham.FastQC.Modules.Per Base Quality Scores. process Sequence (Per Base Quality Scores. jaVA:141)
    at uk.ac.graham. FastQC.Analysis.Analysis Runner.run(Analysis Runner.java:89)
    at java. lang.Thread.run(Thread.java:748)


    The strange thing is that thru the same data it worked ones so either I have somehow damaged the data or I am doing something wrong without realizing it.

    I would really appreciate some help and I thank you for stopping by and reading my post
    Last edited by Robo; 01-25-2020, 06:08 AM.
  • GenoMax
    Senior Member
    • Feb 2008
    • 7142

    #2
    How are you running the fastqc program? You re running out of memory.

    If you are using the bat file on windows then be sure to edit that and increase the value for memory allocation by changing the number in "Xmx2g" to say "Xmx8g". Do not use > 80% of RAM that you actually have.

    Comment

    • Robo
      Junior Member
      • Jan 2020
      • 3

      #3
      Originally posted by GenoMax View Post
      How are you running the fastqc program? You re running out of memory.

      If you are using the bat file on windows then be sure to edit that and increase the value for memory allocation by changing the number in "Xmx2g" to say "Xmx8g". Do not use > 80% of RAM that you actually have.
      Thank you for the quick reply I am running fastqc in a Ubuntu server from the terminal, the resources are allocated based on the needs of the program. Normally it was not giving problems for resources even because the server is quite powerful.
      ______total __|__used___|__free___|shared____|_buff/cache__|_available|
      Mem: |503909_| 283348__|__8718_|__296_____| 211842_____|___217920 |
      Swap:_____0______0________0_____
      the free -m command is giving me the up stated results. I read in a previous topic in here regarding fastqc that sometimes (when you have damaged the data some how) it tries to read files as a single line and thou runes out of memory but I do not know if this is my case.
      Thank you very much
      Last edited by Robo; 01-25-2020, 06:29 AM.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        If you feel your files have become corrupt you can use "validateFiles" utility from Jim Kent to verify the files. Add execute permissions after you download the program. "chmod u+x validateFiles".

        Comment

        • Robo
          Junior Member
          • Jan 2020
          • 3

          #5
          Dear GenoMax, Thank you for the help my files do not have errors despite one being an inode/symlink. at this point, I do not know what the error maybe and I'll write to my supervisor for an appointment.
          Thank you again, and all the best.

          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
          17 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-14-2026, 05:39 AM
          0 responses
          26 views
          0 reactions
          Last Post SEQadmin2  
          Started by SEQadmin2, 10-13-2026, 09:56 AM
          0 responses
          22 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...