Population-specific reference panel improves imputation quality for genome-wide association studies conducted on the Japanese population
Open Access
- 19 December 2024
- journal article
- research article
- Published by Springer Nature in Communications Biology
- Vol. 7 (1) , 1-10
Abstract
To improve imputation quality for genome-wide association studies (GWAS) conducted on the Japanese population, we developed and evaluated four Japanese population-specific reference panels. These panels were constructed through the augmentation of the 1000 Genomes Project (1KG) panel using Japanese whole genome sequencing (WGS) data, with sample sizes ranging from 1 K to 7 K individuals enrolled through the Biobank Japan (BBJ) project, and sequencing depths ranging from 3× to 30×. Among these panels, an augmented reference panel comprising 7472 WGS samples of mixed depth (1KG+7K) exhibit the greatest improvement in imputation quality relative to the Trans-Omics for Precision Medicine (TOPMed) reference panel. Notably, we observe these improvements primarily for rare variants with a minor allele frequency (MAF) P < 5 × 10–8) in the 1KG+7K imputation output yet remaining undetected when the same sample set is imputed up to the TOPMed reference panel. In summary, the 1KG+7K panel demonstrates significant advantages in the discovery of trait-associated loci, particularly those influenced by low-frequency association signals.Keywords
All Related Versions
Funding Information
- Japan Agency for Medical Research and Development (22ek0109555, 21ck0106642, 23ek0410114, 23tm0424225, JP18km0605001)
This publication has 50 references indexed in Scilit:
- RNF213 Variants, Vasospastic Angina, and Risk of Fatal Myocardial InfarctionJAMA Cardiology, 2024
- High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 triosCell, 2022
- Functional characterization of human organic anion transporter 10 (OAT10/SLC22A13) as an orotate transporterDrug Metabolism and Pharmacokinetics, 2022
- Eight novel susceptibility loci and putative causal variants in atopic dermatitisJournal of Allergy and Clinical Immunology, 2021
- Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal herniasEBioMedicine, 2021
- Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicineJournal of Advanced Research, 2021
- Overview of the BioBank Japan Project: Study design and profileJournal of Epidemiology, 2017
- Genotype Imputation with Millions of Reference SamplesThe American Journal of Human Genetics, 2016
- Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designsEuropean Journal of Human Genetics, 2014
- Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’European Journal of Human Genetics, 2014