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  • sohnic
    Junior Member
    • Mar 2011
    • 6

    #1

    tophat - solexa options

    Hi,
    Does anyone known where to find information about the following tophat options:
    --solexa-quals
    --solexa1.3-quals

    I have to align fastq reads (100 nt) issued from a “Hi-Seq 2000” on a reference genome. The data analysis pipeline is HiSeq Control Soft. v. 1.1.37.8 RTA 1.7.48 CASAVA 1.7. So, I'm not sure that the option solexa-quals is the good one in my case ("TopHat was designed to work with reads produced by the Illumina Genome Analyzer").

    Thank you,

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

    #2
    Are you familiar with the three (sequence space) FASTQ variants? See:
    http://dx.doi.org/10.1093/nar/gkp1137

    The type of quality scores from Solexa/Illumunia changed in v1.3 from Solexa to PHRED (different log mappings), and their FASTQ encoding will change again in CASAVA v1.8 to the original Sanger style.
    Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

    Comment

    • sohnic
      Junior Member
      • Mar 2011
      • 6

      #3
      Hi,
      Thanks a lot for those very interesting informations.
      So, I thing I have to use the solexa1.3-quals option in my case.
      To be sure, I've asked the sequencing society. I'm waiting their answer...

      Thanks again for your help,

      S.

      Comment

      • ttnguyen
        Member
        • Mar 2010
        • 41

        #4
        It might be helpful to check the encoding by looking at your FASTQ files. fastQC can do that very quick.

        Comment

        • sohnic
          Junior Member
          • Mar 2011
          • 6

          #5
          Hi,
          The sequencing compagny confirms the use of the solexa1.3-quals option.
          And, fastQC, that seems to be a really good application says the same thing (solexa>1.3).
          Many thanks !

          S.

          Comment

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