A genotype imputation reference panel specific for native Southeast Asian populations

We report the development of a "Southeast Asian Specific (SEA-specific) Reference Panel" through a "Cross-panel Imputation" approach, consisting of 2550 samples derived from the GA100K, SG10K, and the Peninsular Malaysia Orang Asli (OA) datasets, covering 113,851,450 variants. The SEA-specific panel produced more high confidence variants than 1000 Genomes Project (1KGP) when imputing the OA (8.9 million SEA-specific vs 8.1 million 1KGP) and the Singapore Genome Variation Project (SGVP) (12.5 million SEA-specific vs 11.8 million 1KGP) genotyping datasets. Further, the SEA-specific panel imputed SNPs with better estimated quality scores (INFO, DR2 and R<sup>2</sup>) on the OA genotyping dataset when comparing with TOPMED and the Human Genome Diversity Project, but performed similarly on SGVP dataset. This panel also exhibited higher recall and non-reference disconcordance rates, indicating the influence of ancestry closeness of the reference panel. However, we note that the imputation accuracy may be compromised by the size of the reference panel.

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Publication Details

Journal
npj Genomic Medicine
Published
2024-10-05
DOI
https://doi.org/10.1038/s41525-024-00435-7
Citations
6
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
3.30

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article

A genotype imputation reference panel specific for native Southeast Asian populations

Shuhua Xu, Boon‐Peng Hoh, Chee‐Onn Leong, Alvin Cengnata et al.
6 citations
npj Genomic Medicine
Genetic Associations and Epidemiology
3.30
article

A genotype imputation reference panel specific for native Southeast Asian populations

Shuhua Xu, Boon‐Peng Hoh, Chee‐Onn Leong, Alvin Cengnata, Wai-Sum Yap, Lian Deng, Lay-Hong Renee Lim
article en
6 citations

Abstract

We report the development of a "Southeast Asian Specific (SEA-specific) Reference Panel" through a "Cross-panel Imputation" approach, consisting of 2550 samples derived from the GA100K, SG10K, and the Peninsular Malaysia Orang Asli (OA) datasets, covering 113,851,450 variants. The SEA-specific panel produced more high confidence variants than 1000 Genomes Project (1KGP) when imputing the OA (8.9 million SEA-specific vs 8.1 million 1KGP) and the Singapore Genome Variation Project (SGVP) (12.5 million SEA-specific vs 11.8 million 1KGP) genotyping datasets. Further, the SEA-specific panel imputed SNPs with better estimated quality scores (INFO, DR2 and R<sup>2</sup>) on the OA genotyping dataset when comparing with TOPMED and the Human Genome Diversity Project, but performed similarly on SGVP dataset. This panel also exhibited higher recall and non-reference disconcordance rates, indicating the influence of ancestry closeness of the reference panel. However, we note that the imputation accuracy may be compromised by the size of the reference panel.

npj Genomic MedicineVol. 9(1)
Ministry of Health (MY), Fudan University (CN), ShanghaiTech University (CN), ID Genomics (United States) (US), Zhongshan Hospital (CN), UCSI University (MY)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Genetic Associations and Epidemiology
3.30
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