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  • zack80.liu
    Junior Member
    • Feb 2011
    • 9

    #1

    What is this format? How to run bowtie on it.

    I am a newbie to NGS. Please help.

    I have the following file (I was told that it is a export file of illumina)

    HWUSI-EAS1744 1 8 1 1165 18707 0 1 CAACAACTCACCTGCCGAACCAACTAGCTCTGACAACCGATGTCAATCGAACATCGGACGCAATGGAGAACAACG BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB NM N
    HWUSI-EAS1744 1 8 1 1166 9747 0 1 GGCAAGCCGGATCCGTAACTTCGGGATAAGGATTGGCTCTAAGGGCTGGGTCGGTCGGGCTGGGGCGCGAAGCGG bbbbbbabbbbbbbbbbbbbbbbbabbbbb`_bbbbbbbbbbbbbbbbbba`bb__bbb[W]`^^BBBBBBBBBB 0:0:1 Y

    Q1: How do I convert this to fastaq format?
    Q2: Is bbbbbbabbbbbbbbbbbbbbbbbabbbbb`_bbbbbbbbbbbbbbbbbba`bb__bbb[W]`^^BBBBBBBBBB the quality score?
    Q3: How to run bowtie on this file.

    Thanks.
  • HSJD19
    Junior Member
    • Dec 2010
    • 3

    #2
    Format

    This is an export file.
    HWUSI-EAS1744181116518700 1 - Unique Read Identifier
    CAACAACTCACCTGCCGAACCAACTAGCTCTGACAACCGATGTCAATCGAACATCGGACGCAATGGAGAACAACG - Sequence

    BBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBBB - Quality Score in Illumina Platform

    N - The Y or N in the last column is from the Illumina CHASITY filter. Y means yes it pass N means no . I don't think you should use the N sequences.

    Comment

    • HSJD19
      Junior Member
      • Dec 2010
      • 3

      #3
      Might I also suggest reading this thread
      New here? Stop in and introduce yourself. Where you are, what you work on, etc.

      Comment

      • zack80.liu
        Junior Member
        • Feb 2011
        • 9

        #4
        Thanks for the reply.

        Comment

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