In article <DIx4xr.F9t at gpu.utcc.utoronto.ca> lamoran at gpu.utcc.utoronto.ca (L.A. Moran) writes:
Much cogent stuff.
Anyway, we have recently been toying with the idea of using GS in annelids.
I have concerns about introns...
are they likely to be large?
Are you using mRNA template or DNA template?
Ad interim, I am persuing actin (well, a 650 bp portion thereof), but
would like another gene.
Quite frankly I am tired of the 18S. Just too wierd in alignments and
I refuse to delete 1/3 of the data set.
Mark E. Siddall "I don't mind a parasite...
mes at vims.edu I object to a cut-rate one"
Virginia Inst. Marine Sci. - Rick
Gloucester Point, VA, 23062