Genome Medicine (Oct 2019)

NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants

  • Seong-Keun Yoo,
  • Chang-Uk Kim,
  • Hie Lim Kim,
  • Sungjae Kim,
  • Jong-Yeon Shin,
  • Namcheol Kim,
  • Joshua Sung Woo Yang,
  • Kwok-Wai Lo,
  • Belong Cho,
  • Fumihiko Matsuda,
  • Stephan C. Schuster,
  • Changhoon Kim,
  • Jong-Il Kim,
  • Jeong-Sun Seo

DOI
https://doi.org/10.1186/s13073-019-0677-z
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 10

Abstract

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Abstract Here, we present the Northeast Asian Reference Database (NARD), including whole-genome sequencing data of 1779 individuals from Korea, Mongolia, Japan, China, and Hong Kong. NARD provides the genetic diversity of Korean (n = 850) and Mongolian (n = 384) ancestries that were not present in the 1000 Genomes Project Phase 3 (1KGP3). We combined and re-phased the genotypes from NARD and 1KGP3 to construct a union set of haplotypes. This approach established a robust imputation reference panel for Northeast Asians, which yields the greatest imputation accuracy of rare and low-frequency variants compared with the existing panels. NARD imputation panel is available at https://nard.macrogen.com/.

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