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  • SillyPoint
    Member
    • May 2008
    • 39

    #1

    PacBioEDA: Exploratory Data Analysis tools for PacBio RS

    I've just posted to github PacBioEDA, a package of python scripts for subread-level examination of the output of the PacBio instrument.

    From the blurb (on pacbiodevnet, registration required):

    Do you want to have a closer look at the data your PacBio RS
    instrument is producing? Do you want to see a lower level of detail
    than that contained in the reports produced by SMRTanalysis? The
    PacBioEDA package lets you do exploratory data analysis at the
    subread/region level.

    For example: a given read was split into 5 subreads. Each subread
    aligned nicely -- but all of them to the reverse strand, rather than
    in the +-+-+ sequence you'd expect. Looking further, we see that the
    aligned portion of each subread included only the first first half of
    it. Conjecture: we're miscalling the adapter on one end of the
    SMRTbell. Graph the alignment scores for the read against the adapter
    sequence. Conjecture confirmed.

    (The above problem went away with the 1.2.3 release, which does
    a better job of recognising adapters.)

    PacBioEDA consists of a set of python scripts, which accept as input a
    bas.h5 file, and in some cases the associated cmp.h5 alignments file. The
    scripts are run from the command line, and produce either a text file
    or a .png plot as output. This is a no-frills package intended for
    people who are willing to get dirty with their data.

    I've included lots of commentary in the scripts themselves (unlike
    most Open Source bioinformatics offerings, where the only comment is
    the copyright notice), in the hope that this will help you understand
    what the scripts are telling you about your data.

    Tom Skelly ([email protected])
  • SillyPoint
    Member
    • May 2008
    • 39

    #2
    Bug fix for PacBioEDA

    I've just uploaded (link in OP) a fix to PacBioEDA for a bug which caused PacBio_Bas.py to print reference chromosome/contig numbers which do not reflect the order of the chrs in the reference file. It was printing an internal representation that is pretty useless for analysis purposes.

    There are a few improvements as well since I originally uploaded the package. See the CHANGELOG file.

    --TS

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