The use of fluorescence quenching and energy transfer in DNA hybridization
assays is reviewed. Placement of DNA probe labels within interacting distan
ces by hybridization of DNA probes to target DNA or to one another allows r
apid homogeneous analysis of specific DNA sequences. Due to the inherently
lower sensitivity relative to heterogeneous assays, the fluorescence assays
have been coupled with DNA amplification methods such as PCR to provide hi
ghly sensitive, clinically relevant homogeneous assays which can be perform
ed in closed systems.