Wasson Jon, Skolnick Gary, Love-Gregory Latisha, Permutt M Alan
Washington University School of Medicine, Division of Endocrinology, Diabetes, and Metabolism, St. Louis, MO 63110, USA.
Biotechniques. 2002 May;32(5):1144-6, 1148, 1150 passim. doi: 10.2144/02325dd04.
Single nucleotide polymorphism (SNP) association studies searching for differences in allele frequencies between cases and controls have been widely used for genetic analysis. Individual genotyping is prohibitively expensive in large sample sizes. Pooling of samples provides the obvious advantage of higher throughput and lower cost. Here we report our results with the analysis of SNP allele frequencies in DNA pools using Pyrosequencing technology. For seven different SNPs, we observed a mean difference of 1.1 +/- 0.6% between allele frequencies determined in two different DNA pools (n = 150 cases and 150 controls) compared to individually genotyped samples.
寻找病例组和对照组等位基因频率差异的单核苷酸多态性(SNP)关联研究已广泛用于基因分析。在大样本量中进行个体基因分型成本高得令人望而却步。样本合并具有高通量和低成本的明显优势。在此,我们报告使用焦磷酸测序技术分析DNA池中的SNP等位基因频率的结果。对于七个不同的SNP,与个体基因分型样本相比,我们观察到在两个不同的DNA池(n = 150例病例和150例对照)中确定的等位基因频率之间平均差异为1.1 +/- 0.6%。