Two groups have come to the conclusion that breakthroughs in translational medicine require collecting large-scale data on patients, including outcomes, and making those data available to translational researchers. Sage Bionetworks launched a portal through which users can contribute their own health and genomic data for research, and a report from the U.S. National Academy of Sciences is calling for the creation of a national infrastructure for accessing and analyzing open-source patient data.
CITATION STYLE
Kotz, J. (2012). Bringing patient data into the open. Science-Business EXchange, 5(25), 644–644. https://doi.org/10.1038/scibx.2012.644
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