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NARD: whole-genome reference panel of 1779 Northeast Asians improves imputation accuracy of rare and low-frequency variants.
Yoo, Seong-Keun; Kim, Chang-Uk; Kim, Hie Lim; Kim, Sungjae; Shin, Jong-Yeon; Kim, Namcheol; Yang, Joshua Sung Woo; Lo, Kwok-Wai; Cho, Belong; Matsuda, Fumihiko; Schuster, Stephan C; Kim, Changhoon; Kim, Jong-Il; Seo, Jeong-Sun.
Afiliação
  • Yoo SK; Precision Medicine Center, Seoul National University Bundang Hospital, 172 Dolma-ro, Seongnam, Bundang-gu, Gyeonggi-do, 13605, Republic of Korea.
  • Kim CU; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Kim HL; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Kim S; Department of Biomedical Sciences, Seoul National University Graduate School, Seoul, Republic of Korea.
  • Shin JY; The Asian School of the Environment, Nanyang Technological University, Singapore, Singapore.
  • Kim N; Singapore Centre for Environmental Life Sciences Engineering, Nanyang Technological University, Singapore, Singapore.
  • Yang JSW; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Lo KW; Department of Biomedical Sciences, Seoul National University Graduate School, Seoul, Republic of Korea.
  • Cho B; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Matsuda F; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Schuster SC; Precision Medicine Institute, Macrogen Inc., Seongnam, Republic of Korea.
  • Kim C; Department of Anatomical & Cellular Pathology and State Key Laboratory of Translational Oncology, The Chinese University of Hong Kong, Hong Kong, China.
  • Kim JI; Department of Family Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Seo JS; Center for Genomic Medicine, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Genome Med ; 11(1): 64, 2019 10 22.
Article em En | MEDLINE | ID: mdl-31640730
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Polimorfismo de Nucleotídeo Único / Povo Asiático / Estudo de Associação Genômica Ampla / Sequenciamento Completo do Genoma / Genética Populacional Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genoma Humano / Polimorfismo de Nucleotídeo Único / Povo Asiático / Estudo de Associação Genômica Ampla / Sequenciamento Completo do Genoma / Genética Populacional Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article