Cláudia M.B. Carvalho, Sérgio D.J. Pena
Published April 13, 2005
Genet. Mol. Res. 4 (2): 115-125 (2005)

About the Authors
Cláudia M.B. Carvalho, Sérgio D.J. Pena

Corresponding author
S.D.J. Pena
Email: spena@dcc.ufmg.br

ABSTRACT

Several technologically sophisticated high-throughput techniques have been recently developed for the study of human single nucleotide polymorphisms and the diagnosis of point mutations in human diseases. However, there is also a need for simple and inexpensive techniques suitable for clinical services and small research laboratories. Minisequencing meets the latter requirements. It is simple, non-radioactive and can be easily multiplexed by adding oligonucleotide tails of increasing size to the sequencing oligonucleotide primers. To optimize the minisequencing protocol, we designed a test multiplex system capable of typing simultaneously 12 different human autosomal single nucleotide polymorphisms. We discovered that the quality of minisequencing primers and the careful selection of the tail sequences were especially critical for success. This optimized protocol permits rapid genotyping at low cost and can serve as a blueprint for the creation of multiplex minisequencing systems suitable to virtually any typing application in population studies and medical genetics.

Key words: DNA, Polymorphisms, Single nucleotide polymorphisms, Minisequencing, Multiplex.