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 http://www.bi.up.ac.za/~fourie/flowgram.jpg\).

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

Has anyone else experienced something like this?

Any info would be appreciated.

Kindest regards!

Fourie

--------------
Prof Fourie Joubert
Associate Professor
Bioinformatics and Computational Biology Unit
Department of Biochemistry
University of Pretoria
fjoubert@postino.up.ac.za
http://www.bi.up.ac.za
Tel. +27-12-420-5802
Fax. +27-12-420-5800