| Literature DB >> 9514777 |
J Cheng1, L C Waters, P Fortina, G Hvichia, S C Jacobson, J M Ramsey, L J Kricka, P Wilding.
Abstract
Random amplification of the human genome using the degenerate oligonucleotide primed-polymerase chain reaction (DOP-PCR) was performed in a silicon-glass chip. An aliquot of the DOP-PCR amplified genomic DNA was then introduced into another silicon-glass chip for a locus-specific, multiplex PCR of the dystrophin gene exons in order to detect deletions causing Duchenne/Becker muscular dystrophy. Amplicons were analyzed by both conventional capillary electrophoresis and microchip electrophoresis and results were compared to those obtained using standard non-chip-based PCR assays. Results from microchip electrophoresis were consistent with those from conventional capillary electrophoresis. Whole genome amplification products obtained by DOP-PCR proved to be a suitable template for multiplex PCR as long as amplicon size was < 250 bp. Successful detection and resolution of all PCR products from the multiplex PCR clearly shows the feasibility of performing complex PCR assays using microfabricated devices.Entities:
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Year: 1998 PMID: 9514777 DOI: 10.1006/abio.1997.2531
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365