Association testing by DNA pooling: An effective initial screen

被引:122
作者
Bansal, A
van den Boom, D
Kammerer, S
Honisch, C
Adam, G
Cantor, CR
Kleyn, P
Braun, A
机构
[1] SEQUENOM Inc, San Diego, CA 92121 USA
[2] SEQUENOM AB, S-75106 Uppsala, Sweden
[3] SEQUENOM Geminini Ltd, Cambridge CB4 0GH, England
关键词
D O I
10.1073/pnas.262671399
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With an ever-increasing resource of validated single-nucleotide polymorphisms (SNPs), the limiting factors in genome-wide association analysis have become genotyping capacity and the availability of DNA. We provide a proof of concept of the use of pooled DNA as a means of efficiently screening SNPs and prioritizing them for further study. This approach reduces the final number of SNPs that undergo full, sample-by-sample genotyping as well as the quantity of DNA used overall. We have examined 15 SNPs in the cholesteryl ester transfer protein (CETP) gene, a gene previously demonstrated to be associated with serum high-density lipoprotein cholesterol levels. The SNPs were amplified in two pools of DNA derived from groups of individuals with extremely high and extremely low serum high-density lipoprotein cholesterol levels, respectively. P values <0.05 were obtained for 14 SNPs, supporting the described association. Genotyping of the individual samples showed that the average margin of error in frequency estimate was approximate to4% when pools were used. These findings clearly demonstrate the potential of pooling techniques and their associated technologies as an initial screen in the search for genetic associations.
引用
收藏
页码:16871 / 16874
页数:4
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