TY - JOUR
T1 - Imputation disparities driven by recent selection and their impact on disease risk estimation in East and Southeast Asian populations
AU - Li, Dingyang
AU - Tangtanatakul, Pattarin
AU - Lei, Yao
AU - Liu, Xiaoxi
AU - Huang, Hsi Yuan
AU - Lin, Yang Chi Dung
AU - Li, Chengjia
AU - Chen, Yidan
AU - Cai, Lizhi
AU - Zhao, Jinglu
AU - Pisitkul, Prapaporn
AU - Suangtamai, Thanitta
AU - Yu, Jinhan
AU - Zhou, Yihang
AU - Xu, Yuan
AU - Xiao, Yue
AU - Kunhapan, Punna
AU - Sun, Rui
AU - Yu, Guangjun
AU - Sun, Hao
AU - Hirankarn, Nattiya
AU - Ishikawa, Yuki
AU - Terao, Chikashi
AU - Kim, Kwangwoo
AU - Bae, Sang Cheol
AU - Wang, Meiying
AU - Huang, Hsien Da
AU - Yang, Wanling
AU - Wang, Yong Fei
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Accurate genotype imputation is essential for large-scale genetic studies and precision medicine. While East Asian (EAS)-specific reference panels like ChinaMAP and CHN100k have been developed, most studies still rely on multi-ancestry panels like TOPMed due to the large sample size. However, their performance in underrepresented groups like Southeast Asians remains unclear. Using high-coverage whole-genome sequencing and SNP-array data from 8,316 Chinese and Thai individuals, we systematically evaluate six state-of-the-art reference panels for genotype imputation. Our results show that EAS-specific panels outperformed multi-ancestry panels for East and Southeast Asian populations. For example, ChinaMAP achieves a mean heterozygosity concordance rate above 0.90 without R2 filtering, whereas TOPMed requires an R2 threshold of 0.60-0.70 to achieve comparable results. Notably, we find that recent positive selection drives regional disparities in imputation accuracy, as illustrated by the olfactory receptor gene cluster. More importantly, our results indicate that the choice of reference panel and R2 thresholds have a significant impact on polygenic risk score estimation for disease prediction. These findings provide valuable guidelines for improving genotype imputation in East and Southeast Asian populations and underscore the need for ancestrally diverse reference panels to support globally equitable genomic research.
AB - Accurate genotype imputation is essential for large-scale genetic studies and precision medicine. While East Asian (EAS)-specific reference panels like ChinaMAP and CHN100k have been developed, most studies still rely on multi-ancestry panels like TOPMed due to the large sample size. However, their performance in underrepresented groups like Southeast Asians remains unclear. Using high-coverage whole-genome sequencing and SNP-array data from 8,316 Chinese and Thai individuals, we systematically evaluate six state-of-the-art reference panels for genotype imputation. Our results show that EAS-specific panels outperformed multi-ancestry panels for East and Southeast Asian populations. For example, ChinaMAP achieves a mean heterozygosity concordance rate above 0.90 without R2 filtering, whereas TOPMed requires an R2 threshold of 0.60-0.70 to achieve comparable results. Notably, we find that recent positive selection drives regional disparities in imputation accuracy, as illustrated by the olfactory receptor gene cluster. More importantly, our results indicate that the choice of reference panel and R2 thresholds have a significant impact on polygenic risk score estimation for disease prediction. These findings provide valuable guidelines for improving genotype imputation in East and Southeast Asian populations and underscore the need for ancestrally diverse reference panels to support globally equitable genomic research.
UR - https://www.scopus.com/pages/publications/105026163084
U2 - 10.1038/s42003-025-09214-1
DO - 10.1038/s42003-025-09214-1
M3 - Article
C2 - 41272119
AN - SCOPUS:105026163084
SN - 2399-3642
VL - 8
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 1822
ER -