From genomic databases to translation: a call to action

Journal of Medical Ethics 37 (8):515-516 (2011)

Authors
R. Douglas Cox
University of Western Australia
Abstract
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
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DOI 10.1136/jme.2011.043042
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