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  • seqador
    Junior Member
    • Aug 2013
    • 9

    #1

    Error using fastqc

    I get 8 sra files that was converted to fastq. The first fastq file was successfully analysed with fastqc. But after that all files after 100% get this error:


    Approx 90% complete for SRR1503281_1.fastq
    Approx 95% complete for SRR1503281_1.fastq
    Approx 100% complete for SRR1503281_1.fastq
    Exception in thread "Thread-1" java.lang.NullPointerException
    at uk.ac.babraham.FastQC.Sequence.FastQFile.readNext(FastQFile.java:141)
    at uk.ac.babraham.FastQC.Sequence.FastQFile.next(FastQFile.java:105)
    at uk.ac.babraham.FastQC.Analysis.AnalysisRunner.run(AnalysisRunner.java:76)
    at java.lang.Thread.run(Thread.java:744)




    could someone know why this is happening? Thank you.
    Last edited by seqador; 08-01-2014, 08:31 PM.
  • Cytosine
    Member
    • Mar 2014
    • 22

    #2
    Code:
    Exception in thread "Thread-1" java.lang.NullPointerException
    at uk.ac.babraham.FastQC.Sequence.FastQFile.readNext(FastQFile.java:141)
    at uk.ac.babraham.FastQC.Sequence.FastQFile.next(FastQFile.java:105)
    at uk.ac.babraham.FastQC.Analysis.AnalysisRunner.run(AnalysisRunner.java:76)
    This makes me think that FastQC cannot go to the next file simply because it can't find it in memory. Do you call fastqc on all files at once or do it 1 by 1?

    Try 1 by 1 if you're feeding all at once to fastqc now.

    If that is not the case, maybe try redownloading the sra files and extracting them again.

    Comment

    • seqador
      Junior Member
      • Aug 2013
      • 9

      #3
      I try your two suggestions, and try 1 by 1 solve the problem. But i wish to do all files with a single command.
      Last edited by seqador; 08-02-2014, 04:27 AM.

      Comment

      • GenoMax
        Senior Member
        • Feb 2008
        • 7142

        #4
        You need to run FastQC in non-interactive mode (on command line) to overcome running out of memory.

        You could simply do

        Code:
        $ /path_to_/fastqc sequence_file*.fastq
        This should produce a self contained folder for each sequence file with all the result you normally see via GUI.

        Comment

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