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The Data Use Ontology to streamline responsible access to human biomedical datasets.
Lawson, Jonathan; Cabili, Moran N; Kerry, Giselle; Boughtwood, Tiffany; Thorogood, Adrian; Alper, Pinar; Bowers, Sarion R; Boyles, Rebecca R; Brookes, Anthony J; Brush, Matthew; Burdett, Tony; Clissold, Hayley; Donnelly, Stacey; Dyke, Stephanie O M; Freeberg, Mallory A; Haendel, Melissa A; Hata, Chihiro; Holub, Petr; Jeanson, Francis; Jene, Aina; Kawashima, Minae; Kawashima, Shuichi; Konopko, Melissa; Kyomugisha, Irene; Li, Haoyuan; Linden, Mikael; Rodriguez, Laura Lyman; Morita, Mizuki; Mulder, Nicola; Muller, Jean; Nagaie, Satoshi; Nasir, Jamal; Ogishima, Soichi; Ota Wang, Vivian; Paglione, Laura D; Pandya, Ravi N; Parkinson, Helen; Philippakis, Anthony A; Prasser, Fabian; Rambla, Jordi; Reinold, Kathy; Rushton, Gregory A; Saltzman, Andrea; Saunders, Gary; Sofia, Heidi J; Spalding, John D; Swertz, Morris A; Tulchinsky, Ilia; van Enckevort, Esther J; Varma, Susheel.
Afiliação
  • Lawson J; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Cabili MN; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Kerry G; European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
  • Boughtwood T; Australian Genomics, Murdoch Children's Research Institute, Parkville, VIC, Australia.
  • Thorogood A; Centre of Genomics and Policy, Department of Human Genetics, McGill University, Montreal, QC, Canada.
  • Alper P; ELIXIR-Luxembourg, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.
  • Bowers SR; ELIXIR-Luxembourg, Luxembourg Centre for Systems Biomedicine, University of Luxembourg, Belvaux, Luxembourg.
  • Boyles RR; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Brookes AJ; RTI International, Research Triangle Park, NC, USA.
  • Brush M; University of Leicester, Leicester, UK.
  • Burdett T; University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Clissold H; European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
  • Donnelly S; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
  • Dyke SOM; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Freeberg MA; McGill Centre for Integrative Neuroscience, Montreal Neurological Institute, Department of Neurology & Neurosurgery, Faculty of Medicine, McGill University, Montreal, QC, Canada.
  • Haendel MA; European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
  • Hata C; University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Holub P; Bioinformation and DDBJ Center, National Institute of Genetics, Mishima, Japan.
  • Jeanson F; BBMRI-ERIC, AT and Masaryk University, Brno, Czech Republic.
  • Jene A; University Health Network, Toronto, ON, Canada.
  • Kawashima M; Centre de Regulació Genòmica (CRG), Barcelona, Spain.
  • Kawashima S; National Bioscience Database Center, Japan Science and Technology Agency, Tokyo, Japan.
  • Konopko M; Database Center for Life Science, Joint Support-Center for Data Science Research, Research Organization of Information and Systems, Kashiwa, Japan.
  • Kyomugisha I; ELIXIR Hub, Wellcome Genome Campus, Hinxton, UK.
  • Li H; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Linden M; Canada's Michael Smith Genome Sciences Centre, Vancouver, BC, Canada.
  • Rodriguez LL; ELIXIR-Finland, CSC - IT Center for Science Ltd, Espoo, Finland.
  • Morita M; Patient-Centered Outcomes Research Institute, Washington, DC, USA.
  • Mulder N; Okayama University, Okayama, Japan.
  • Muller J; Computational Biology Division, IDM, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
  • Nagaie S; Laboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace, INSERM U1112, Université; de Strasbourg, Strasbourg, France.
  • Nasir J; Laboratoire de Diagnostic Génétique, Institut de Génétique Médicale d'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Ogishima S; Tohoku Medical Megabank Organization (ToMMo), Tohoku University, Sendai, Japan.
  • Ota Wang V; Department of Life Sciences, University of Northampton, Northampton, UK.
  • Paglione LD; Tohoku Medical Megabank Organization (ToMMo), Tohoku University, Sendai, Japan.
  • Pandya RN; Office of Data Sharing, National Cancer Institute, NIH, Rockville, MD, USA.
  • Parkinson H; Spherical Cow Group, Rego Park, NY 11374, USA.
  • Philippakis AA; Microsoft Research, Redmond, WA 98052, USA.
  • Prasser F; European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
  • Rambla J; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Reinold K; Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Rushton GA; Centre de Regulació Genòmica (CRG), Barcelona, Spain.
  • Saltzman A; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Saunders G; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Sofia HJ; Broad Institute of Harvard and the Massachusetts Institute of Technology, Cambridge, MA, USA.
  • Spalding JD; ELIXIR Hub, Wellcome Genome Campus, Hinxton, UK.
  • Swertz MA; National Human Genome Research Institute, NIH, Bethesda, MD, USA.
  • Tulchinsky I; European Molecular Biology Laboratory-European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
  • van Enckevort EJ; Genomics Coordination Center, Department of Genetics, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands.
  • Varma S; Google Cloud, Kitchener, ON N2H 5G5, Canada.
Cell Genom ; 1(2): None, 2021 Nov 10.
Article em En | MEDLINE | ID: mdl-34820659
ABSTRACT
Human biomedical datasets that are critical for research and clinical studies to benefit human health also often contain sensitive or potentially identifying information of individual participants. Thus, care must be taken when they are processed and made available to comply with ethical and regulatory frameworks and informed consent data conditions. To enable and streamline data access for these biomedical datasets, the Global Alliance for Genomics and Health (GA4GH) Data Use and Researcher Identities (DURI) work stream developed and approved the Data Use Ontology (DUO) standard. DUO is a hierarchical vocabulary of human and machine-readable data use terms that consistently and unambiguously represents a dataset's allowable data uses. DUO has been implemented by major international stakeholders such as the Broad and Sanger Institutes and is currently used in annotation of over 200,000 datasets worldwide. Using DUO in data management and access facilitates researchers' discovery and access of relevant datasets. DUO annotations increase the FAIRness of datasets and support data linkages using common data use profiles when integrating the data for secondary analyses. DUO is implemented in the Web Ontology Language (OWL) and, to increase community awareness and engagement, hosted in an open, centralized GitHub repository. DUO, together with the GA4GH Passport standard, offers a new, efficient, and streamlined data authorization and access framework that has enabled increased sharing of biomedical datasets worldwide.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article