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J-GLOBAL ID：201602212824432974   Reference number：16A0008801

Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals

ジャポニカアレイ:1070人の日本人を対象にした住民集団特異的なSNPアレーのデザインによる遺伝子型帰属の改善

Author (9)： KAWAI Yosuke (Tohoku Univ., Sendai, JPN) ,  MIMORI Takahiro (Tohoku Univ., Sendai, JPN) ,  KOJIMA Kaname (Tohoku Univ., Sendai, JPN) ,  NARIAI Naoki (Tohoku Univ., Sendai, JPN) ,  DANJOH Inaho (Tohoku Univ., Sendai, JPN) ,  SAITO Rumiko (Tohoku Univ., Sendai, JPN) ,  YASUDA Jun (Tohoku Univ., Sendai, JPN) ,  YAMAMOTO Masayuki (Tohoku Univ., Sendai, JPN) ,  NAGASAKI Masao (Tohoku Univ., Sendai, JPN)
Material： Journal of Human Genetics  (J Hum Genet)
Volume： 60  Issue： 10  Page： 581-587  Publication year： Oct. 2015 
JST Material Number： Z0756A  ISSN： 1434-5161  Document type： Article
Article type： 原著論文  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： DNA microarray ,...
Semi thesaurus term： *pharmacogenomics ,...

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JST classification (2)： Molecular genetics in general  (EC02010J) ,  Pharmacology in general  (GW01000B)

Reference (23)：

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• Marchini, J. & Howie, B. Genotype imputation for genome-wide association studies. Nat. Rev. Genet. 11, 499-511 (2010).
• Holm, H., Gudbjartsson, D. F., Sulem, P., Masson, G., Helgadottir, H. T., Zanon, C. et al. A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Nat. Genet. 43, 316-320 (2011).
• Steinthorsdottir, V., Thorleifsson, G., Sulem, P., Helgason, H., Grarup, N., Sigurdsson, A. et al. Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes. Nat. Genet. 46, 294-298 (2014).
• The 1000 Genomes Project Consortium. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56-65 (2012).

Terms in the title (8)： ジャポニカアレイ ,  日本人 ,  住民 ,  集団 ,  SNP ,  アレー ,  デザイン ,  遺伝子型