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Journal article

Enabling global clinical collaborations on identifiable patient data: The Minerva Initiative

Abstract:

The clinical utility of computational phenotyping for both genetic and rare diseases is increasingly appreciated; however, its true potential is yet to be fully realized. Alongside the growing clinical and research availability of sequencing technologies, precise deep and scalable phenotyping is required to serve unmet need in genetic and rare diseases. To improve the lives of individuals affected with rare diseases through deep phenotyping, global big data interrogation is necessary to aid o...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.3389/fgene.2019.00611

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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Role:
Author
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Publisher:
Frontiers Media Publisher's website
Journal:
Frontiers in Genetics Journal website
Volume:
10
Pages:
611
Publication date:
2019-07-29
Acceptance date:
2019-06-12
DOI:
EISSN:
1664-8021
Source identifiers:
1036931
Keywords:
Pubs id:
pubs:1036931
UUID:
uuid:c7123389-1d80-4f3c-ac11-81876354cfc8
Local pid:
pubs:1036931
Deposit date:
2019-08-01

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