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The rapid rise of international collaborative science has enabled access to genomic data. In this article, it is argued that to move beyond mapping genomic variation to understanding its role in complex disease aetiology and treatment will require extending data sharing for the purposes of clinical research translation and implementation.

Original publication

DOI

10.1136/jme.2011.043042

Type

Journal article

Journal

Journal of Medical Ethics

Publication Date

01/08/2011

Volume

37

Pages

515 - 516