The analysis of DNA extracted from archival clinical specimens using polyme
rase chain reaction represents the basis of a variety of research and diagn
ostic protocols in medicine. However, the selection of optimal DNA extracti
on method is critical if such an analysis is to be successful. Recently, we
have evaluated a number of rapid DNA extraction protocols in order to find
the most suitable method for routine processing of the most common archiva
l materials in pathological and cytological laboratories: paraffin-embedded
tissues and Papanicolaou- or Giemsa-stained smears, Our results demonstrat
e that rapid DNA extraction methods have comparable DNA extraction efficien
cies with standard DNA isolation protocols on archival clinical specimens w
ith the exception of Giemsa-stained smears.