Sharing clinical and genomic data on cancer - The need for global solutions

New England Journal of Medicine

Volumn 376, Issue 21, 2017, Pages 2006-2009

  Lawler, Mark ^a   Haussler, David ^b   Siu, Lillian L ^c   McMurry, Julie A ^d   Knoppers, Bartha M ^e   Chanock, Stephen J ^f   Calvo, Fabien ^g   The, Bin T ^h   Walia, Guneet ⁱ   Banks, Ian ^j   Yu, Peter P ^k   Staudt, Louis M ^f   Sawyers, Charles L ^l  

^a QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^b University of California Santa Cruz   (United States)

^c UNIVERSITY OF TORONTO   (Canada)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^e MCGILL UNIVERSITY   (Canada)

^f NATIONAL CANCER INSTITUTE   (United States)

^g Institute Gustave Roussy Cancer Campus   (France)

^h DIVISION OF MEDICAL ONCOLOGY   (Singapore)

ⁱ Bonnie J Addario Lung Cancer Foundation   (United States)

^j European Cancer Organization Patient Advocacy Committee   (Belgium)

^k Hartford HealthCare Cancer Institute   (United States)

^l MEMORIAL SLOAN KETTERING CANCER CENTER   (United States)

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Author keywords

[No Author keywords available]

Indexed keywords

ACCESS TO INFORMATION; CANCER GENETICS; CANCER RESEARCH; CLOUD COMPUTING; COMPUTER SECURITY; DATA ANALYSIS; ELECTRONIC MEDICAL RECORD; FINANCIAL MANAGEMENT; GENOTYPE PHENOTYPE CORRELATION; HUMAN; INFORMATION PROCESSING; INFORMATION RETRIEVAL; INTERNATIONAL COOPERATION; MALIGNANT NEOPLASM; MEDICAL INFORMATION; MEDICAL RESEARCH; PERSONALIZED MEDICINE; POLICY; PRIORITY JOURNAL; PRIVACY; QUALITY CONTROL; REVIEW; ETHICS; GENETICS; GENOMICS; INFORMATION DISSEMINATION; LEGISLATION AND JURISPRUDENCE; NEOPLASM;

GENOMICS; HUMANS; INFORMATION DISSEMINATION; INTERNATIONAL COOPERATION; NEOPLASMS;

EID: 85019953273     PISSN: 00284793     EISSN: 15334406     Source Type: Journal    
DOI: 10.1056/NEJMp1612254     Document Type: Review

References (5)

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3. Vis DJ, Lewin J, Liao RG, et al. Towards a global cancer knowledge network: dissecting the current international cancer genomic sequencing landscape. Ann Oncol 2017; 28: 1145-51.
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5. Dewey FE, Murray MF, Overton JD, et al. Distribution and clinical impact of functional variants in 50, 726 whole-exome sequences from the DiscovEHR study. Science 2016; 354: aaf6814.