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Registered access: authorizing data access

Authors :
Dyke, Stephanie O.M.
Linden, Mikael
Lappalainen, Ilkka
De Argila, Jordi R.
Carey, Knox
Lloyd, David
Spalding, J.D.
Cabili, Moran N.
Kerry, Giselle
Foreman, Julia
Cutts, Tim
Shabani, Mahsa
Rodriguez, Laura L.
Haeussler, Maximilian
Walsh, Brian
Jiang, Xiaoqian
Wang, Shuang
Perrett, Daniel
Boughtwood, Tiffany
Matern, Andreas
Brookes, Anthony J.
Cupak, Miro
Fiume, Marc
Pandya, Ravi
Tulchinsky, Ilia
Scollen, Serena
Törnroos, Juha
Das, Samir
Evans, Alan C.
Malin, Bradley A.
Beck, Stephan
Brenner, Steven E.
Nyrönen, Tommi
Blomberg, Niklas
Firth, Helen V.
Hurles, Matthew
Philippakis, Anthony A.
Rätsch, Gunnar
Brudno, Michael
Boycott, Kym M.
Rehm, Heidi L.
Baudis, Michael
Sherry, Stephen T.
Kato, Kazuto
Knoppers, Bartha M.
Baker, Dixie
Flicek, Paul
Publisher :
ETH Zurich

Abstract

The Global Alliance for Genomics and Health (GA4GH) proposes a data access policy model—“registered access”—to increase and improve access to data requiring an agreement to basic terms and conditions, such as the use of DNA sequence and health data in research. A registered access policy would enable a range of categories of users to gain access, starting with researchers and clinical care professionals. It would also facilitate general use and reuse of data but within the bounds of consent restrictions and other ethical obligations. In piloting registered access with the Scientific Demonstration data sharing projects of GA4GH, we provide additional ethics, policy and technical guidance to facilitate the implementation of this access model in an international setting.<br />European Journal of Human Genetics, 26 (12)<br />ISSN:1476-5438<br />ISSN:1018-4813

Subjects

Subjects :
3. Good health

Details

Language :
English
ISSN :
14765438 and 10184813
Database :
OpenAIRE
Accession number :
edsair.doi...........e4ed96fa5e1c845e9c611d5442308c0c