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精细遗传结构和罕见变异频率。

Fine-scale genetic structure and rare variant frequencies.

机构信息

Département des Sciences Fondamentales, Université du Québec à Chicoutimi, Saguenay, Québec, Canada.

Centre Intersectoriel en Santé Durable, Université du Québec à Chicoutimi, Saguenay, Québec, Canada.

出版信息

PLoS One. 2024 Nov 5;19(11):e0313133. doi: 10.1371/journal.pone.0313133. eCollection 2024.

Abstract

In response to the current challenge in genetic studies to make new associations, we advocate for a shift toward leveraging population fine-scale structure. Our exploration brings to light distinct fine-structure within populations having undergone a founder effect such as the Ashkenazi Jews and the population of the Quebec' province. We leverage the fine-scale population structure to explore its impact on the frequency of rare variants. Notably, we observed an 8-fold increase in frequency for a variant associated with the Usher syndrome in one Quebec subpopulation. Our study underscores that smaller cohorts with greater genetic similarity demonstrate an important increase in rare variant frequencies, offering a promising avenue for new genetic variants' discovery.

摘要

针对当前遗传研究中发现新关联的挑战,我们主张转向利用人群精细结构。我们的探索揭示了经历过奠基者效应的人群(如阿什肯纳兹犹太人以及魁北克省的人群)中存在明显的精细结构。我们利用精细的人口结构来探索其对罕见变异频率的影响。值得注意的是,我们观察到一个与 Usher 综合征相关的变异在魁北克一个亚群中的频率增加了 8 倍。我们的研究强调了具有更大遗传相似性的较小队列中罕见变异频率的重要增加,为新的遗传变异的发现提供了有前途的途径。

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