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  • arrchi
    Member
    • Mar 2011
    • 46

    #1

    fastQC output question

    Hi there,

    Here is one of the reports from fastQC. In the per_base_quality plot, the first 11 bases look weird. I wonder if I need to trim the first 11 bases? And possible reasons?

    Thank a bunch.
    Attached Files
    Last edited by arrchi; 08-30-2012, 10:40 AM.
  • JQL
    Member
    • Apr 2011
    • 83

    #2
    mine look quite similar to yours. So I have same questions.
    The QC suggests it passed. I wonder what is the recommended passing score? 30? what standard they use to make the pass/fail call?

    thanks

    Originally posted by arrchi View Post
    Hi there,

    Here is one of the reports from fastQC. In the per_base_quality plot, the first 11 bases look weird. I wonder if I need to trim the first 11 bases? And possible reasons?

    Thank a bunch.

    Comment

    • kmcarr
      Senior Member
      • May 2008
      • 1181

      #3
      arrchi,

      Your plot is a perfectly normal (and good) plot for Illumina HiSeq data. For whatever reason the Q-score prediction algorithm in the HiSeq RTA stair steps the quality scores over the first 13 bases (3-5-5).

      Comment

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