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  • rahularjun86
    Member
    • Jan 2011
    • 58

    #1

    Reads quality scoring system used ??

    Dear all,
    As most of the NGS data analysis packages(Bowtie2, Sickle,...) depends on the reads quality scores, Is there any tool/package to predict the quality scores used for the raw reads?? I was trying this with unix grep and then checking the ASCII tables for ranges used in my raw reads.
    Many thanks,
    Rahul
    Rahul Sharma,
    Ph.D
    Frankfurt am Main, Germany
  • chadn737
    Senior Member
    • Jan 2009
    • 392

    #2
    What sequencing platform?

    Comment

    • rahularjun86
      Member
      • Jan 2011
      • 58

      #3
      I have two lanes of paired end Illumina reads. One lane sequenced after 1 and half year. Using grep, I am getting symbols having ASCII value staring from 35 in lane1(Phred quality score) and in another lane the values are starting from 64(Illumina 1.3+).
      Rahul Sharma,
      Ph.D
      Frankfurt am Main, Germany

      Comment

      • chadn737
        Senior Member
        • Jan 2009
        • 392

        #4
        Starting with CASAVA 1.5+ used phred+64 but with CASAVA 1.8 they switched to phred+33.

        Check out this thread:

        Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

        Comment

        • Heisman
          Senior Member
          • Dec 2010
          • 534

          #5
          If you run it through FastQC it will output the quality score system it detected.

          Also maybe look here: https://www.uppnex.uu.se/content/che...y-score-format

          Comment

          • rahularjun86
            Member
            • Jan 2011
            • 58

            #6
            Dear Heisman and chadn737,
            Many thanks for your great help, I will try these methods soon.
            Best regards,
            Rahul
            Rahul Sharma,
            Ph.D
            Frankfurt am Main, Germany

            Comment

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