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  • hujiacun
    Member
    • Mar 2015
    • 17

    #1

    why the read sequence from IGV can't be found in fastq?

    I found a strange read pair from IGV, so i want to extract the original information about the read pair.
    I use " zcat file.fastq.gz | grep -B 3 "TCTCAAAAAGCACATGGATTCTACTCCTGATTTCTCCAAGGATCTACATATGATCAAAACATATCTTTACCAGATTCTCCGTGGAATTGCGTATTGCCACTCTCATAGGGTTCTCCATCGTGATC"
    The strange thing is i can't find it in original fq file.
  • dpryan
    Devon Ryan
    • Jul 2011
    • 3478

    #2
    Try grepping for the read name, that's less error prone:

    Code:
    zgrep -A 3 "HWI:stuff" file.fastq.gz

    Comment

    • maubp
      Peter (Biopython etc)
      • Jul 2009
      • 1544

      #3
      My guess is the sequence has been reverse complemented, and that's why you can't find it. As dpryan suggests, try searching by the read name instead.

      Comment

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