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  • UNCKidney
    Junior Member
    • Apr 2010
    • 5

    Tophat Segment-based junction error = -9

    [Tue Apr 6 12:18:12 2010] Beginning TopHat run (v1.0.13)
    -----------------------------------------------
    [Tue Apr 6 12:18:12 2010] Preparing output location ./tophat_out/
    [Tue Apr 6 12:18:12 2010] Checking for Bowtie index files
    [Tue Apr 6 12:18:12 2010] Checking for reference FASTA file
    Warning: Could not find FASTA file hg19.fa
    [Tue Apr 6 12:18:12 2010] Reconstituting reference FASTA file from Bowtie index
    [Tue Apr 6 13:34:32 2010] Checking for Bowtie
    Bowtie version: 0.12.3.0
    [Tue Apr 6 13:34:32 2010] Checking reads
    seed length: 37bp
    format: fastq
    quality scale: phred33 (default)
    [Tue Apr 6 13:47:18 2010] Mapping reads against hg19 with Bowtie
    [Tue Apr 6 15:22:25 2010] Joining segment hits
    [Tue Apr 6 15:30:27 2010] Searching for junctions via segment mapping
    [FAILED]
    Error: segment-based junction search failed with err = -9




    Not sure what happened and what error 9 means anyone have an idea ? Let me know if I should post any log files, this is my first time using Tophat
  • sunnyvu
    Member
    • Mar 2010
    • 17

    #2
    From the report you provided, "Warning: Could not find FASTA file hg19.fa", I think you should make sure the index file is ok.

    Comment

    • UNCKidney
      Junior Member
      • Apr 2010
      • 5

      #3
      I think it reconstituted it afterwards from the bowtie indexes, should I have downloaded them from EMBL or NCBI instead ? The fasta genome files that is.

      Comment

      • sunnyvu
        Member
        • Mar 2010
        • 17

        #4
        Try this one:
        When the first running finished, the fasta file was reconstituted into output fold, then move the fasta file from the output fold into index fold.

        Comment

        • sunnyvu
          Member
          • Mar 2010
          • 17

          #5
          Try the following:
          I guess the file has been created into the output fold. For the next running, try to move the fasta file into the index fold.

          Comment

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