| Literature DB >> 11140947 |
B Hoogendoorn1, N Norton, G Kirov, N Williams, M L Hamshere, G Spurlock, J Austin, M K Stephens, P R Buckland, M J Owen, M C O'Donovan.
Abstract
At present, the cost of genotyping single nucleotide polymorphisms (SNPs) in large numbers of subjects poses a formidable problem for molecular genetic approaches to complex diseases. We have tested the possibility of using primer extension and denaturing high performance liquid chromatography to estimate allele frequencies of SNPs in pooled DNA samples. Our data show that this method should allow the accurate estimation of absolute allele frequencies in pooled samples of DNA and also of the difference in allele frequency between different pooled DNA samples. This technique therefore offers an efficient and cheap method for genotyping SNPs in large case-control and family-based association samples.Mesh:
Substances:
Year: 2000 PMID: 11140947 DOI: 10.1007/s004390000397
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132