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PLoS Genet. 2016 Jan 21;12(1):e1005772. doi: 10.1371/journal.pgen.1005772. eCollection 2016 Jan.

Consent Codes: Upholding Standard Data Use Conditions.

Author information

1
Centre of Genomics and Policy, Faculty of Medicine, McGill University, Montreal, Quebec, Canada.
2
Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.
3
Centre for Genomic Regulation (CRG), Barcelona, Spain.
4
Universitat Pompeu Fabra (UPF), Barcelona, Spain.
5
Office of Science Policy, Office of the Director, National Institutes of Health, Bethesda, Maryland, United States of America.
6
Department of Genetics, University of Leicester, Leicester, United Kingdom.
7
European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton, Cambridge, United Kingdom.
8
Human Genetics Department, Leiden University Medical Center, Leiden, The Netherlands.
9
Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
10
Centre for Computational Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.
11
Department of Computer Science, University of Toronto, Toronto, Ontario, Canada.
12
Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, United Kingdom.
13
Department of Pathology, Brigham & Women's Hospital and Harvard Medical School, Boston, Massachusetts, United States of America.
14
Bioreference Laboratories, Inc., Elmwood Park, New Jersey, United States of America.
15
DNAstack, Toronto, Ontario, Canada.
16
National Centre for Biotechnology Information, US National Library of Medicine, Bethesda, Maryland, United States of America.

Abstract

A systematic way of recording data use conditions that are based on consent permissions as found in the datasets of the main public genome archives (NCBI dbGaP and EMBL-EBI/CRG EGA).

PMID:
26796797
PMCID:
PMC4721915
DOI:
10.1371/journal.pgen.1005772
[Indexed for MEDLINE]
Free PMC Article

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