| Literature DB >> 11968087 |
J Ross Hawkins1, Yuri Khripin, Ana M Valdes, Thomas A Weaver.
Abstract
DNA diagnostics has been progressively moving from expensive, low-throughput, multi-step methods towards inexpensive, robust, and high-throughput methods. Here we describe the further validation and refinement of a recently described novel genotyping method that has the latter characteristics. An evolved form of allele-specific PCR, the method generates a fluorescent signal through the use of universal labeled primers, which can be quantified directly from microplates using standard plate readers. We have applied the method successfully to a test set of 12 novel single nucleotide polymorphisms (SNPs) on a panel of 47 individuals using low reaction volumes. We demonstrate that the method is extremely accurate, robust, and can be optimized in a simple and predictable manner. By conducting the assay in closed-tube format, the potential for contamination is reduced to a minimum. By virtue of its simplicity, the method is versatile and cost-effective with potential for use in industrial-scale genetic studies or in the clinical diagnostic setting. Copyright 2002 Wiley-Liss, Inc.Mesh:
Substances:
Year: 2002 PMID: 11968087 DOI: 10.1002/humu.10060
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878