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Association testing by DNA pooling: An effective initial screen

机译:DNA合并的关联测试:有效的初始筛选

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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 ≈4% 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.
机译:随着越来越多的经过验证的单核苷酸多态性(SNP)资源,全基因组关联分析中的限制因素已成为基因分型能力和DNA的可用性。我们提供了使用合并的DNA作为有效筛选SNP并确定其优先级以进行进一步研究的手段的概念证明。这种方法减少了经过完整的逐样本基因分型的SNP的最终数量,以及整体使用的DNA数量。我们已经检查了胆固醇酯转移蛋白(CETP)基因中的15个SNP,该基因先前已证明与血清高密度脂蛋白胆固醇水平相关。在分别来自具有极高和极低血清高密度脂蛋白胆固醇水平的个体的组的两个DNA池中扩增了SNP。获得14个SNP的P值<0.05,支持上述关联。各个样本的基因分型表明,使用池时,频率估计的平均误差范围约为≈4%。这些发现清楚地证明了合并技术及其相关技术作为寻找遗传关联的初始筛选的潜力。

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