Sharma Shivam, Nagar Shashwat Deepali, Pemu Priscilla, Zuchner Stephan, Mariño-Ramírez Leonardo, Meller Robert, Jordan I King
School of Biological Sciences, Georgia Institute of Technology, Atlanta, GA, USA.
National Institute on Minority Health and Health Disparities, National Institutes of Health, Bethesda, MD, USA.
Nat Commun. 2025 May 3;16(1):4123. doi: 10.1038/s41467-025-59351-8.
We analyzed participant genomic variant data to characterize population structure and genetic ancestry for the All of Us cohort (n = 297,549). There is substantial population structure in the cohort, with clusters of closely related participants interspersed among less related individuals. Participants show diverse genetic ancestry, with major contributions from European (66.4%), African (19.5%), Asian (7.6%), and American (6.3%) continental ancestry components. Participant genetic similarity clusters show group-specific ancestry, with distinct patterns of continental and subcontinental ancestry among groups. African and American ancestry are enriched in the southeast and southwest regions of the country, respectively, whereas European ancestry is more evenly distributed across the US. The diversity of All of Us participants' genetic ancestry is negatively correlated with age; younger participants show higher levels of genetic admixture compared to older participants. Our results underscore the ancestral genetic diversity of the All of Us cohort, a crucial prerequisite for genomic health equity.
我们分析了参与者的基因组变异数据,以描述“我们所有人”队列(n = 297,549)的群体结构和遗传血统。该队列存在显著的群体结构,亲缘关系密切的参与者群体散布于亲缘关系较远的个体之中。参与者呈现出多样的遗传血统,主要源自欧洲(66.4%)、非洲(19.5%)、亚洲(7.6%)和美洲(6.3%)大陆的血统成分。参与者的遗传相似性群体显示出特定群体的血统,不同群体之间存在大陆和次大陆血统的独特模式。非洲和美洲血统分别在美国东南部和西南部地区更为集中,而欧洲血统在美国各地分布更为均匀。“我们所有人”参与者的遗传血统多样性与年龄呈负相关;与年长参与者相比,年轻参与者表现出更高水平的遗传混合。我们的结果强调了“我们所有人”队列的祖先遗传多样性,这是基因组健康公平的关键先决条件。