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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fine-scale genetic structure and rare variant frequencies

Catherine Laprise, Laurence Gagnon, Simon Girard, Claudia Moreau
6 citations
PLoS ONE
Genetic Associations and Epidemiology
3.30
article

Fine-scale genetic structure and rare variant frequencies

Catherine Laprise, Laurence Gagnon, Simon Girard, Claudia Moreau
article en
6 citations

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.

PLoS ONEVol. 19(11)
Université du Québec à Chicoutimi (CA), Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean (CA), Université Laval (CA)
Alliance de recherche numérique du Canada, Canadian Institutes of Health Research
Openalex Percentile: Top 7%
Genetic Associations and Epidemiology
3.30
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.