A method is presented for the analysis of fluorescently labeled random
amplified polymorphic DNA (FRAPD) fragments. A DNA sequencer and coll
ection and analysis software were used to estimate the sizes of DNA fr
agments based on their mobilities relative to in-lane size markers. Th
is allowed confident identification and comparison of FRAPD markers bo
th within and between polyacrylamide gels. In comparison with analysis
of RAPD products using ethidium bromide-stained agarose gels, fluores
cent analysis Improved the sensitivity, resolution and precision of si
zing of RAPD products of about 50-2100 bp. FRAPD fragments produced fr
om amplification of zebrafish DNA are informative as genetic markers t
hat segregate with Mendelian inheritance. FRAPD analysis was found to
be very efficient for identifying new DNA polymorphisms.