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  • frymor
    Senior Member
    • May 2010
    • 151

    bowtie output

    Hi,

    I'm running bowtie with this command:
    bowtie -a --best --strata -m 10 -n 2 -l 22 -q --un mut.unmapped -t -p 2 -5 11 --chunkmbs 256 --max mut.maxHits -S d_melanogaster_fb5_32 -1 s2_1_sequence.fq -2 s2_2_sequence.fq output.sam
    this what I am getting on my output when I am running bowtie:
    Time loading reference: 00:00:01
    Time loading forward index: 00:00:01
    Time loading mirror index: 00:00:01
    Seeded quality full-index search: 05:03:50
    # reads processed: 42867915
    # reads with at least one reported alignment: 21891058 (51.07%)
    # reads that failed to align: 20748783 (48.40%)
    # reads with alignments suppressed due to -m: 228074 (0.53%)
    Reported 23418877 paired-end alignments to 1 output stream(s)
    Time searching: 05:03:53
    Overall time: 05:03:53
    For each of the paired-end fastq files I have 42867915 reads. this is also the sum of the three #-lines.
    What is the meaning of the number in the last line? -23418877

    Thanks
    Assa
  • andrehorta
    Member
    • Jan 2011
    • 14

    #2
    I don't know too.

    Process C:/ufmg/brca_diagnostic/FASTQ/SRR062634.filt.fastq
    # reads processed: 308846
    # reads with at least one reported alignment: 833 (0.27%)
    # reads that failed to align: 308013 (99.73%)
    Reported 833 alignments to 1 output stream(s)
    # reads processed: 308846
    # reads with at least one reported alignment: 794 (0.26%)
    # reads that failed to align: 308052 (99.74%)
    Reported 794 alignments to 1 output stream(s)
    Look for mutations...

    Comment

    • csoong
      Member
      • Jun 2009
      • 74

      #3
      Seems like some PE-reads were mapped to more than 1 location but below your "m" threshold.

      Comment

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