精细遗传结构和罕见变异频率

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2024-11-05 eCollection Date: 2024-01-01 DOI:10.1371/journal.pone.0313133
Laurence Gagnon, Claudia Moreau, Catherine Laprise, Simon L Girard
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引用次数: 0

摘要

为了应对当前基因研究在建立新联系方面所面临的挑战,我们主张转向利用人群的精细结构。我们的探索揭示了经历过创始效应的人群(如阿什肯纳兹犹太人和魁北克省的人群)中独特的精细结构。我们利用精细的种群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,在一个魁北克亚人群中,与乌谢尔综合征相关的变体频率增加了 8 倍。我们的研究强调,遗传相似性更高的小型队列会显著增加罕见变异的频率,这为发现新的遗传变异提供了一个前景广阔的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fine-scale genetic structure and rare variant frequencies.

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.

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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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