Does anyone know if
1) it is possible to use gap to align
the whole of the consensus sequence to a sequence in the database.
I am having trouble using the Align algorithm because it does not seem
to align the whole of the sequence.
2) Also is it possible to use gap to take in ABI files without having to
convert them to scf or exp files, since having ABI and other file
formats takes up alot of disk space.
3) If you have more than 36 sequences in a single contig is there a way
that you could scroll down to look at your sequences or is the only way
of doing this is to get a 17 or 20" screen?
4) When you use VEPE to screen against a vector, can you get a
chromatogram with the vector sequence left out and just your internal
sequence in a separate chromatogram.
rifat at icr.ac.uk