Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Genetic Associations and Epidemiology

The International HapMap Project

Nature · 2003

RRichard A. Gibbs·JJohn W. Belmont·PPaul Hardenbol·TT. D. Willis·FFuli Yu·HHuanming Yang·LLan-Yang Ch'ang·WWei Huang·BBin Liu·YYan Shen·PPaul Kwong Hang Tam·LLap-Chee Tsui·MMary Miu Yee Waye·JJ. Tze‐Fei Wong·CChangqing Zeng·QQingrun Zhang·IIllumina·MMark S. Chee·LLuana Galver·SSemyon Kruglyak·SSarah S. Murray·AArnold Oliphant·AAlexandre Montpetit·TThomas J. Hudson·FFanny Chagnon·VVincent Ferretti·MMartin Leboeuf·MMichael Phillips·AAndrei Verner·PPui-Yan Kwok·SShenghui Duan·DDenise L. Lind·RRaymond D. Miller·JJohn P. Rice·NNancy L. Saccone·PPatricia Taillon‐Miller·MMing Xiao·YYusuke Nakamura·AAkihiro Sekine·KKoki Sorimachi·TToshihiro Tanaka·YYoïchi Tanaka·TTatsuhiko Tsunoda·EEiji Yoshino·DDavid Bentley·PPanos Deloukas·SSarah Hunt·DDon Powell·DDavid Altshuler·SStacey B. Gabriel·HHoucan Zhang·IIchiro Matsuda·YYoshimitsu Fukushima·DDarryl Macer·EEiko Suda·CCharles N. Rotimi·CClement Adebamowo·TToyin Aniagwu·PPatricia A. Marshall·OOlayemi Matthew·CChibuzor Nkwodimmah·CCharmaine D. M. Royal·MMark Leppert·MMissy Dixon·LLincoln D. Stein·FFiona Cunningham·AArdavan Kanani·GGuðmundur Á. Þórisson·AAravinda Chakravarti·PPeter E. Chen·DDavid J. Cutler·CCarl Kashuk·PPeter Donnelly·JJonathan Marchini·GGil McVean·SSimon Myers·LLon R. Cardon·GGonçalo R. Abecasis·AAndrew P. Morris·BBruce S. Weir·JJames C. Mullikin·SStephen T. Sherry·MMichael Feolo·MMark Daly·SStephen F. Schaffner·RRen-Zong Qiu·GGenetic Interest Group·AAlastair Kent·GGeorgia M. Dunston·KKazuto Kato·NNorio Niikawa·BBartha Maria Knoppers·MMorris W. Foster·EEllen Wright Clayton·VVivian Ota Wang·WWellcome Trust·JJessica Watkin
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Abstract

The goal of the International HapMap Project is to determine the common patterns of DNA sequence variation in the human genome and to make this information freely available in the public domain. An international consortium is developing a map of these patterns across the genome by determining the genotypes of one million or more sequence variants, their frequencies and the degree of association between them, in DNA samples from populations with ancestry from parts of Africa, Asia and Europe. The HapMap will allow the discovery of sequence variants that affect common disease, will facilitate development of diagnostic tools, and will enhance our ability to choose targets for therapeutic intervention.

Research topics