Zimmermann J, Wiemann S, Voss H, Schwager C, Ansorge W
European Molecular Biology Laboratory, Heidelberg, FRG.
Biotechniques. 1994 Aug;17(2):302, 304, 306 passim.
Recently available thermostable DNA polymerases result in enhanced resolution and accuracy compared to thermal enzymes used previously in fluorescent cycle sequencing. These new enzymes produce less variations in peak intensities, enhance gel resolution and are less sensitive to unspecific termination caused by either DNA structure or impurities in the DNA preparation. Optimization of nucleotide ratios and the usage of high concentrations of detergents in the sequencing reaction result in sequence readings up to 1000 bases and improve overall reliability of the sequencing protocol; this works successfully in about 90% of cases.