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  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #31
    Originally posted by guo View Post
    Hi. everyone.

    Should we transform the fastq file from solid2fastq (Bfast) before mapping with bwa?
    I mean from "0123123" to "ACTGACT", something likewise plus some other format issues?

    Before, I proced without any transformation, then got malformed .sai file and some "segmentation fault" which I haven't specified yet.

    Any suggestions? Thank you
    Make sure you use the solid2fastq within BWA if you are going to use BWA. On the other hand, if you are using bfast+bwa, make sure you see the command line parameters in BFAST's solid2fastq.

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    • nilshomer
      Nils Homer
      • Nov 2008
      • 1283

      #32
      Originally posted by NanYu View Post
      I'm wondering in the postprocess step, if BFAST will do something like: choose the best for F and second best for R within a pair because that is within the expected distance, yet the best for R is in another chromsome.
      I know it is a rare scenario and maybe I should not worry about it.
      It could happen when using the insert size distance in the probability calculation, though it is rare.

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