We have just gotten the staden package. I went to a training course for
gap4 at George Mason U. and was very impressed with it. We will be using
it with both bacterial and human sequencing projects. We will be using
phred for generating the base scores. I was wondering if any one has
advice for me. Are there common pitfalls to aviod when setting this up,
or features that I may miss that are very useful, or advice on making
data available. My thoughts are that we'll make both the sequence and
scores available, but I'm not sure if people would finds that of use.
Any advice will be useful,
ps. why are there so many get rich quick schemes on this group?
John J. McNulty (Jack)
Brookhaven National Laboratory
Upton, NY 11973
email: jack at bnl.gov