http://nar.oxfordjournals.org/cgi/content/abstract/29/17/e88

An efficient procedure for genotyping single nucleotide polymorphisms
Shu Ye*, Sahar Dhillon, Xiayi Ke, Andrew R. Collins and Ian N. M. Day
Human Genetics Research Division, University of Southampton, Duthie Building (MP808), Southampton General Hospital, Tremona Road, Southampton SO16 6YD, UK

Analysis of single nucleotide polymorphisms (SNPs) has been and will be increasingly utilized in various genetic disciplines, particularly in studying genetic determinants of complex diseases. Such studies will be facilitated by rapid, simple, low cost and high throughput methodologies for SNP genotyping. One such method is reported here, named tetra-primer ARMS-PCR, which employs two primer pairs to amplify, respectively, the two different alleles of a SNP in a single PCR reaction. A computer program for designing primers was developed. Tetra-primer ARMS-PCR was combined with microplate array diagonal gel electrophoresis, gaining the advantage of high throughput for gel-based resolution of tetra-primer ARMS-PCR products. The technique was applied to analyse a number of SNPs and the results were completely consistent with those from an independent method, restriction fragment length polymorphism analysis.

* To whom correspondence should be addressed. Tel: +44 23 8079 4929
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C. A. Milbury, J. Li, and G. M. Makrigiorgos
PCR-Based Methods for the Enrichment of Minority Alleles and Mutations
Clin. Chem., April 1, 2009; 55(4): 632 - 640.
[Abstract] [Full Text] [PDF]


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J. Li, L. Wang, P. A. Janne, and G. M. Makrigiorgos
Coamplification at Lower Denaturation Temperature-PCR Increases Mutation-Detection Selectivity of TaqMan-Based Real-Time PCR
Clin. Chem., April 1, 2009; 55(4): 748 - 756.
[Abstract] [Full Text] [PDF]