| Literature DB >> 34131746 |
Mika Sakurai-Yageta1,2, Kazuki Kumada1,2, Chinatsu Gocho1, Satoshi Makino1, Akira Uruno1,3, Shu Tadaka1, Ikuko N Motoike1,4, Masae Kimura1, Shin Ito1, Akihito Otsuki1,3, Akira Narita1, Hisaaki Kudo1, Yuichi Aoki1,4, Inaho Danjoh1, Jun Yasuda1, Hiroshi Kawame1, Naoko Minegishi1,2, Seizo Koshiba1,2, Nobuo Fuse1,2,3, Gen Tamiya1,2,3, Masayuki Yamamoto1,2,3, Kengo Kinoshita1,2,4.
Abstract
Ethnic-specific SNP arrays are becoming more important to increase the power of genome-wide association studies in diverse population. In the Tohoku Medical Megabank Project, we have been developing a series of Japonica Arrays (JPA) for genotyping participants based on reference panels constructed from whole-genome sequence data of the Japanese population. Here, we designed a novel version of the SNP array for the Japanese population, called Japonica Array NEO (JPA NEO), comprising a total of 666,883 markers. Among them, 654,246 tag SNPs of autosomes and X chromosome were selected from an expanded reference panel of 3,552 Japanese, 3.5KJPNv2, using pairwise r2 of linkage disequilibrium measures. Additionally, 28,298 markers were included for the evaluation of previously identified disease risk markers from the literature and databases, and those present in the Japanese population were extracted using the reference panel. Through genotyping 286 Japanese samples, we found that the imputation quality r2 and INFO score in the minor allele frequency bin >2.5-5% were >0.9 and >0.8, respectively, and >12 million markers were imputed with an INFO score >0.8. From these results, JPA NEO is a promising tool for genotyping the Japanese population with genome-wide coverage, contributing to the development of genetic risk scores.Entities:
Keywords: Tohoku Medical Megabank Project; disease risk alleles; ethnic-specific SNP array; genome-wide coverage; genotype imputation
Year: 2021 PMID: 34131746 DOI: 10.1093/jb/mvab060
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387