Trev: problem when viewing 454 sff files

  • Hi

    I have two sets of experiments, one from a international company and one done locally.

    When I view the sff flowgrams of the international data in trev, I get a lot of discrepancies of basecall vs. peak color (see\).

    When i view the locally-generated data, everything is perfect...

    Has anyone else experienced something like this?

    Any info would be appreciated.

    Kindest regards!


    Prof Fourie Joubert
    Associate Professor
    Bioinformatics and Computational Biology Unit
    Department of Biochemistry
    University of Pretoria
    Tel. +27-12-420-5802
    Fax. +27-12-420-5800