Integrating common and rare genetic variation in diverse human populations

David M. Altshuler; S. F. Schaffner; Stacey B. Gabriel; Xiaoming Jia; Joshua M. Korn; James Nemesh; Samuela Pollack; Wendy Brodeur; Huy Nguyen; Ilya Shlyakhter; Richard A. Gibbs; Fuli Yu; Penelope E. Bonnen; Kyle Chang; Alicia Hawes; Lora Lewis; Yanru Ren; David A. Wheeler; Donna M. Muzny; Claudia Gonzaga‐Jauregui; Emmanouil T. Dermitzakis; Stephen B. Montgomery; Rhian Gwilliam; Sarah Hunt; Aarno Palotie; Pamela Whittaker; C. Barnes; Kati Kristiansson; Nicole Soranzo; Verneri Anttila; Qingrun Zhang; Mohammed J. R. Ghori; William McLaren; Fumihiko Takeuchi; Katayoon Darvishi; Charles Lee; Alon Keinan; Alkes L. Price; Mark J. Daly; Stephen Leslie; Gil McVean; Loukas Moutsianas; Sharon R. Grossman; Elizabeth B. Hostetter; Clement A. Adebamowo; Morris W. Foster; Deborah R. Gordon; Julio Licinio; Maria Cristina Manca; Patricia A. Marshall; Ichiro Matsuda; Duncan Ngare; Vivian Ota Wang; Deepa Reddy; Charles N. Rotimi; Charmaine D. Royal; Richard R. Sharp; Changqing Zeng; Lisa D. Brooks; Jean E. McEwen

Năm xuất bản2010

Nguồn học thuậtNature

Định danhDOI 10.1038/nature09298

TRÍCH DẪN ĐỀ XUẤTAPA 7

Thông tin thư mục

Nguồn/Tạp chí: Nature
Tập: 467
Số: 7311
Trang: 52-58
Nhà xuất bản: Nature Portfolio
DOI: 10.1038/nature09298 ↗

Từ khóa

International HapMap Project; Single-nucleotide polymorphism; Minor allele frequency; Biology; Imputation (statistics); Genetics; 1000 Genomes Project; Human genetic variation; Haplotype; Human genome; Genetic variation; Tag SNP; Haplotype estimation; Genome-wide association study; Genetic association; Population; Allele frequency; SNP genotyping; Genomics; Allele; Genotype; Genome; Gene; Missing data; Medicine