Evidence map›Paper›PMID 42479736›Full record

ArticlePLoS genetics2026

Multi-ancestry colocalization approaches.

Cathy Shen, Josée Dupuis, Qihuang Zhang

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Cathy ShenDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0009-0006-6381-2518
Josée DupuisDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.
Qihuang ZhangDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0003-1455-2159

Funding

TOPMed Omics of Type 2 Diabetes and Quantitative TraitsUM1DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MANNING, ALISA KNODLE · 2021 to 2025
$3.8M
TOPMed Omics of Cardiovascular Disease in DiabetesR01HL151855 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2020 to 2023
$3.3M
NHLBI NIH HHS R01 HL151855NIDDK NIH HHS UM1 DK078616
6 · The paper itself

Abstract

Genome-wide association studies (GWAS) have identified thousands of variants associated with complex traits, but many are non-causal. Statistical fine-mapping methods aim to pinpoint the most likely causal variants among the many associated ones. While most fine-mapping methods were originally limited to single ancestry analysis, multi-ancestry fine-mapping methods are now available, leveraging differences in linkage disequilibrium (LD) and minor allele frequencies (MAFs) across ancestries to improve fine-mapping resolution. However, the biological relevance of the putative causal variants identified through fine-mapping often remains unclear. Colocalization methods improve interpretability by integrating GWAS data with other functional genomics datasets to assess whether two traits share the same causal variants. Despite the growing availability of multi-ancestry data, there are currently no established methods for multi-ancestry colocalization. In this study, we propose multi-ancestry colocalization approaches through the integration of multi-ancestry fine-mapping methods, SuSiEx and MsCAVIAR, with single ancestry colocalization methods, coloc and eCAVIAR. We introduce coloc_SuSiEx, eCAVIAR_SuSiEx, eMsCAVIAR and coloc_MsCAVIAR. The performance of the proposed approaches is evaluated and compared through simulation studies. In loci with a single causal variant, credible set sizes across the four approaches were comparable, as was the prioritization of the true causal variant. MsCAVIAR-based approaches were more computationally expensive compared to SuSiEx-based approaches, which is an important consideration for the analysis of regions with multiple causal variants. Compared to the coloc-based approaches, the eCAVIAR-based approaches tended to report lower loci level colocalization posterior probabilities. For the analysis of loci with multiple causal variants, coloc_SuSiEx is the preferred approach. We apply the proposed approaches to perform a colocalization analysis of multi-ancestry T2D GWAS data from the DIAMANTE Consortium and European pQTL data from the INTERVAL study. This work addresses the increasing need for multi-ancestry approaches to colocalization analysis as more multi-ancestry data become available.

Indexed as

Chromosome MappingGenome-Wide Association StudyGene FrequencyHumansLinkage DisequilibriumPolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID42479736
PMCPMC13387578

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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.