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Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel

机译:使用具有高度区分性的祖先资料性41-SNP面板推断人类大陆起源和混合比例

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Background Accurate determination of genetic ancestry is of high interest for many areas such as biomedical research, personal genomics and forensics. It remains an important topic in genetic association studies, as it has been shown that population stratification, if not appropriately considered, can lead to false-positive and -negative results. While large association studies typically extract ancestry information from available genome-wide SNP genotypes, many important clinical data sets on rare phenotypes and historical collections assembled before the GWAS area are in need of a feasible method (i.e., ease of genotyping, small number of markers) to infer the geographic origin and potential admixture of the study subjects. Here we report on the development, application and limitations of a small, multiplexable ancestry informative marker (AIM) panel of SNPs (or AISNP) developed specifically for this purpose. Results Based on worldwide populations from the HGDP, a 41-AIM AISNP panel for multiplex application with the ABI SNPlex and a subset with 31 AIMs for the Sequenome iPLEX system were selected and found to be highly informative for inferring ancestry among the seven continental regions Africa, the Middle East, Europe, Central/South Asia, East Asia, the Americas and Oceania. The panel was found to be least informative for Eurasian populations, and additional AIMs for a higher resolution are suggested. A large reference set including over 4,000 subjects collected from 120 global populations was assembled to facilitate accurate ancestry determination. We show practical applications of this AIM panel, discuss its limitations for admixed individuals and suggest ways to incorporate ancestry information into genetic association studies. Conclusion We demonstrated the utility of a small AISNP panel specifically developed to discern global ancestry. We believe that it will find wide application because of its feasibility and potential for a wide range of applications.
机译:背景技术对于许多领域,例如生物医学研究,个人基因组学和法医学,准确确定遗传血统是非常重要的。它已经成为遗传关联研究中的一个重要课题,因为已经表明,如果不适当考虑种群分层,可能导致假阳性和阴性结果。虽然大型关联研究通常从可用的全基因组SNP基因型中提取血统信息,但是有关GWAS之前的罕见表型和历史记录的许多重要临床数据集仍需要一种可行的方法(即,易于进行基因分型,少量标记) )以推断研究对象的地理来源和潜在的混合物。在这里,我们报告专门为此目的开发的SNP(或AISNP)小型可复用祖先信息标记(AIM)面板的开发,应用和局限性。结果根据来自HGDP的全球人口,选择了一个41-AIM AISNP专家组与ABI SNPlex进行多重应用,并将一个带有31个AIM的子集用于Sequenome iPLEX系统,发现该信息对于非洲七个大陆地区的血统推断很有帮助。 ,中东,欧洲,中亚/南亚,东亚,美洲和大洋洲。发现该小组对欧亚人口的信息最少,建议使用其他更高分辨率的AIM。收集了一个大型参考集,其中包括从120个全球人口中收集的4,000多个主题,以帮助准确确定血统。我们展示了这个AIM小组的实际应用,讨论了混合个体的局限性,并提出了将祖先信息纳入遗传关联研究的方法。结论我们展示了专门为识别全球血统而开发的小型AISNP小组的实用性。我们相信,由于它的可行性和广泛应用的潜力,它将得到广泛的应用。

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