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.
Authors
- Catherine Laprise (ORCID: https://orcid.org/0000-0001-5526-9945)
- Laurence Gagnon (ORCID: https://orcid.org/0009-0007-9920-997X)
- Simon Girard (ORCID: https://orcid.org/0000-0002-4089-2280)
- Claudia Moreau (ORCID: https://orcid.org/0000-0002-1480-3045)
Institutions
- Université du Québec à Chicoutimi (CA)
- Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean (CA)
- Université Laval (CA)
Publication Details
- Journal
- PLoS ONE
- Published
- 2024-11-05
- DOI
- https://doi.org/10.1371/journal.pone.0313133
- Citations
- 6
- Primary Topic
- Genetic Associations and Epidemiology
- Type
- article
- Field-Weighted Citation Impact
- 3.30
Funders
- Alliance de recherche numérique du Canada
- Canadian Institutes of Health Research