Evidence map›Paper›PMID 40646547›Full record

ArticleGenome biology2025

Admixed and single-continental genome segments of the same ancestry have distinct linkage disequilibrium patterns.

Hanbin Lee, Moo Hyuk Lee, Kangcheng Hou, Bogdan Pasaniuc, Buhm Han

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Article in Genome biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hanbin Lee *Department of Statistics, University of Michigan, Ann Arbor, MI, USA. hblee@umich.edu.
Moo Hyuk Lee *Department of Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Kangcheng HouDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Bogdan PasaniucDepartment of Genetics, University of Pennsylvania, Philadelphia, PA, USA.
Buhm HanDepartment of Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea. buhm.han@snu.ac.kr.ORCID http://orcid.org/0000-0002-2266-5164

Funding

Methods for Genome-wide Association Studies in Admixed PopulationsR01HG006399 · NHGRI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI PRICE, ALKES L · 2011 to 2024
$6.3M
NHGRI NIH HHS R01 HG006399
6 · The paper itself

Abstract

backgroundAdmixed populations offer valuable insight into the genetic architecture of complex traits. Many studies have proposed methods for genome-wide association study (GWAS) in admixed populations and various simulation studies have evaluated their performances. In this work, we propose another direction of comparison of recently proposed methods for admixed GWAS from a population genetic viewpoint.

resultsOur theoretical approach mathematically and directly compares the power of methods given that the causal variant is tested. This is done by deriving the variance formula of the methods from the population genetic admixture model. Our results analytically confirm previous observation that the standard GWAS test is more powerful than alternative tests due to leveraging allele frequency heterogeneity in which alternatives do not. As a by-product, we obtain a simple method to improve the power of multi-degrees-of-freedom tests only using summary statistics. We further investigate the problem when the causal variant is not directly known but is detected by tagging variants in linkage disequilibrium (LD). The analysis shows that a genetic segment from admixed genomes may exhibit distinct LD patterns from the single-continental counterpart of the same ancestry.

conclusionsWhile the classic admixture model is successful in predicting GWAS power, its popular extension in the literature falls short in explaining the LD patterns found in simulations and real data, warranting an improved model for LD in admixed genomes.

Indexed as

Genome, HumanGenome-Wide Association StudyLinkage DisequilibriumComputer SimulationGene FrequencyGenetics, PopulationHumansModels, GeneticPolymorphism, Single NucleotideAdmixtureGenome-wide association studyPopulation genetics

Identifiers

PMID40646547
PMCPMC12255047

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