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Hum Mutat. 2015 Oct;36(10):985-8. doi: 10.1002/humu.22840. Epub 2015 Aug 27.

Data sharing in the undiagnosed diseases network.

Author information

1
Division of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.
2
Center for Biomedical Informatics, Harvard Medical School, Boston, Massachusetts.
3
Columbia Institute for Genomic Medicine, Genetics and Development, New York, New York.

Abstract

The Undiagnosed Diseases Network (UDN) builds on the successes of the Undiagnosed Diseases Program at the National Institutes of Health (NIH UDP). Through support from the NIH Common Fund, a coordinating center, six additional clinical sites, and two sequencing cores comprise the UDN. The objectives of the UDN are to: (1) improve the level of diagnosis and care for patients with undiagnosed diseases through the development of common protocols designed by an enlarged community of investigators across the network; (2) facilitate research into the etiology of undiagnosed diseases, by collecting and sharing standardized, high-quality clinical and laboratory data including genotyping, phenotyping, and environmental exposure data; and (3) create an integrated and collaborative research community across multiple clinical sites, and among laboratory and clinical investigators, to investigate the pathophysiology of these rare diseases and to identify options for patient management. Broad-based data sharing is at the core of achieving these objectives, and the UDN is establishing the policies and governance structure to support broad data sharing.

KEYWORDS:

Matchmaker Exchange; big data; genetics; genomics; personalized medicine; precision medicine

PMID:
26220576
PMCID:
PMC4706173
DOI:
10.1002/humu.22840
[Indexed for MEDLINE]
Free PMC Article

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