Paltoo Dina N, Rodriguez Laura Lyman, Feolo Michael, Gillanders Elizabeth, Ramos Erin M, Rutter Joni L, Sherry Stephen, Wang Vivian Ota, Bailey Alice, Baker Rebecca, Caulder Mark, Harris Emily L, Langlais Kristofor, Leeds Hilary, Luetkemeier Erin, Paine Taunton, Roomian Tamar, Tryka Kimberly, Patterson Amy, Green Eric D
Nat Genet. 2014 Sep;46(9):934-8. doi: 10.1038/ng.3062.
In 2007, the US National Institutes of Health (NIH) introduced the Genome-Wide Association Studies (GWAS) Policy and the database of Genotypes and Phenotypes (dbGaP) to facilitate 'controlled' access to GWAS data based on participants' informed consent. dbGaP has provided 2,221 investigators access to 304 studies, resulting in 924 publications and significant scientific advances. Following on this success, the 2014 Genomic Data Sharing Policy will extend the GWAS Policy to additional data types.
The online version of this article (doi:10.1038/ng.3062) contains supplementary material, which is available to authorized users.
2007年，美国国立卫生研究院（NIH）推出了全基因组关联研究（GWAS）政策以及基因型和表型数据库（dbGaP），以促进在参与者知情同意的基础上对GWAS数据进行“受控”访问。dbGaP已为2221名研究人员提供了对304项研究的访问权限，产生了924篇出版物和重大的科学进展。在此成功基础上，2014年的基因组数据共享政策将把GWAS政策扩展到其他数据类型。
本文的在线版本（doi:10.1038/ng.3062）包含补充材料，授权用户可获取。
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