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  • cklopp
    Member
    • Sep 2009
    • 12

    #1

    PacBio P6C4 homopolymer error bias

    Using the alignment of the raw pacbio reads on a reference genome it is possible to count the number of insertions and deletions at each position (from the mpileup file) and to sum these figures for homopolymers. It is then possible to calculate the mean error rates per variation type and homopolymer length.

    The results for one of our genomes of interest is presented hereunder.
    We clearly see that the insertion proportion decreases with the homopolymer length and on the contrary the deletion proportion increases.



    NB1 : this genome having only few homopolymers larger than 7 base pairs the corresponding figures have to be taken with caution.

    NB2 : We have the same shapes for other genomes.

    PacBio data is meant to have random errors which does not seem to be true looking at these figures.

    I'm interested in any finding or comment about this issue.
  • dcopetti
    Junior Member
    • Nov 2011
    • 2

    #2
    interesting.
    Does the bias disappear after Pilon polishing with Illumina reads, for example?
    It would be also nice to see a similar analysis about Nanopore data.
    good point, we need to be aware of that

    Comment

    • cklopp
      Member
      • Sep 2009
      • 12

      #3
      Unfortunately I do not have Illumina reads for this genome, I will therefore not be able to answer your pilon related request.
      For Oxford Nanopore we are aware of the evident homopolymer bias.

      Comment

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