» Articles » PMID: 35714612

Leveraging the Local Genetic Structure for Trans-ancestry Association Mapping

Overview
Journal Am J Hum Genet
Publisher Cell Press
Specialty Genetics
Date 2022 Jun 17
PMID 35714612
Authors
Affiliations
Soon will be listed here.
Abstract

Over the past two decades, genome-wide association studies (GWASs) have successfully advanced our understanding of the genetic basis of complex traits. Despite the fruitful discovery of GWASs, most GWAS samples are collected from European populations, and these GWASs are often criticized for their lack of ancestry diversity. Trans-ancestry association mapping (TRAM) offers an exciting opportunity to fill the gap of disparities in genetic studies between non-Europeans and Europeans. Here, we propose a statistical method, LOG-TRAM, to leverage the local genetic architecture for TRAM. By using biobank-scale datasets, we showed that LOG-TRAM can greatly improve the statistical power of identifying risk variants in under-represented populations while producing well-calibrated p values. We applied LOG-TRAM to the GWAS summary statistics of various complex traits/diseases from BioBank Japan, UK Biobank, and African populations. We obtained substantial gains in power and achieved effective correction of confounding biases in TRAM. Finally, we showed that LOG-TRAM can be successfully applied to identify ancestry-specific loci and the LOG-TRAM output can be further used for construction of more accurate polygenic risk scores in under-represented populations.

Citing Articles

A unified framework for cell-type-specific eQTL prioritization by integrating bulk and scRNA-seq data.

Yu X, Hu X, Wan X, Zhang Z, Wan X, Cai M Am J Hum Genet. 2025; 112(2):332-352.

PMID: 39824189 PMC: 11866979. DOI: 10.1016/j.ajhg.2024.12.018.


A comprehensive framework for trans-ancestry pathway analysis using GWAS summary data from diverse populations.

Fu S, Wheeler W, Wang X, Hua X, Godbole D, Duan J PLoS Genet. 2024; 20(10):e1011322.

PMID: 39441834 PMC: 11534268. DOI: 10.1371/journal.pgen.1011322.


Multi-trait GWAS for diverse ancestries: mapping the knowledge gap.

Troubat L, Fettahoglu D, Henches L, Aschard H, Julienne H BMC Genomics. 2024; 25(1):375.

PMID: 38627641 PMC: 11022331. DOI: 10.1186/s12864-024-10293-3.


PGS-Depot: a comprehensive resource for polygenic scores constructed by summary statistics based methods.

Cao C, Zhang S, Wang J, Tian M, Ji X, Huang D Nucleic Acids Res. 2023; 52(D1):D963-D971.

PMID: 37953384 PMC: 10767792. DOI: 10.1093/nar/gkad1029.


XMAP: Cross-population fine-mapping by leveraging genetic diversity and accounting for confounding bias.

Cai M, Wang Z, Xiao J, Hu X, Chen G, Yang C Nat Commun. 2023; 14(1):6870.

PMID: 37898663 PMC: 10613261. DOI: 10.1038/s41467-023-42614-7.


References
1.
DerSimonian R, Laird N . Meta-analysis in clinical trials. Control Clin Trials. 1986; 7(3):177-88. DOI: 10.1016/0197-2456(86)90046-2. View

2.
Hu Y, Lu Q, Powles R, Yao X, Yang C, Fang F . Leveraging functional annotations in genetic risk prediction for human complex diseases. PLoS Comput Biol. 2017; 13(6):e1005589. PMC: 5481142. DOI: 10.1371/journal.pcbi.1005589. View

3.
Link J, Reue K . Genetic Basis for Sex Differences in Obesity and Lipid Metabolism. Annu Rev Nutr. 2017; 37:225-245. PMC: 5759759. DOI: 10.1146/annurev-nutr-071816-064827. View

4.
Zhu X, Stephens M . Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes. Nat Commun. 2018; 9(1):4361. PMC: 6195536. DOI: 10.1038/s41467-018-06805-x. View

5.
Yang C, Li C, Wang Q, Chung D, Zhao H . Implications of pleiotropy: challenges and opportunities for mining Big Data in biomedicine. Front Genet. 2015; 6:229. PMC: 4485215. DOI: 10.3389/fgene.2015.00229. View