Evidence map›Paper›PMID 40162269›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Evaluating Multi-Ancestry Genome-Wide Association Methods: Statistical Power, Population Structure, and Practical Implications.

Julie-Alexia Dias, Tony Chen, Hua Xing, Xiaoyu Wang, Alex A Rodriguez, Ravi K Madduri, Peter Kraft, Haoyu Zhang

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Julie-Alexia DiasDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Tony ChenDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Hua XingDivision of Cancer Epidemiology & Genetics, National Cancer Institute, National Instituters of Health, Bethesda, MD, USA.
Xiaoyu WangDivision of Cancer Epidemiology & Genetics, National Cancer Institute, National Instituters of Health, Bethesda, MD, USA.
Alex A RodriguezData Science and Learning division, Argonne National Laboratory, Lemont, IL, USA.
Ravi K MadduriData Science and Learning division, Argonne National Laboratory, Lemont, IL, USA.
Peter KraftDivision of Cancer Epidemiology & Genetics, National Cancer Institute, National Instituters of Health, Bethesda, MD, USA.
Haoyu ZhangDivision of Cancer Epidemiology & Genetics, National Cancer Institute, National Instituters of Health, Bethesda, MD, USA.ORCID 0000-0001-6423-0444

Funding

Leveraging Prospective Cancer Epidemiology Cohorts and Novel Methods to Improve Polygenic Risk ScoresU01CA261339 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fei Chen, David V Conti · 2021 to 2026
$5.2M
Interdisciplinary training: Statistical Genetics/Genomics and Computational BiologyT32GM135117 · NIGMS · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Curtis Huttenhower, XIHONG LIN · 2020 to 2026
$3.1M
NCI NIH HHS U01 CA261339NIGMS NIH HHS T32 GM135117
6 · The paper itself

Abstract

The increasing availability of diverse biobanks has enabled multi-ancestry genome-wide association studies (GWAS), enhancing the discovery of genetic variants across traits and diseases. However, the choice of an optimal method remains debated due to challenges in statistical power differences across ancestral groups and approaches to account for population structure. Two primary strategies exist: (1) Pooled analysis, which combines individuals from all genetic backgrounds into a single dataset while adjusting for population stratification using principal components, increasing the sample size and statistical power but requiring careful control of population stratification. (2) Meta-analysis, which performs ancestry-group-specific GWAS and subsequently combines summary statistics, potentially capturing fine-scale population structure, but facing limitations in handling admixed individuals. Using large-scale simulations with varying sample sizes and ancestry compositions, we compare these methods alongside real data analyses of eight continuous and five binary traits from the UK Biobank (

Indexed as

All of UsGenome-wide association studiesMeta-analysisPopulation StratificationUK Biobank

Identifiers

PMID40162269
PMCPMC11952640

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.