Open Data in the Era of the GDPR: Lessons from the Human Cell Atlas

Author:

Knoppers Bartha Maria1,Bernier Alexander1,Bowers Sarion2,Kirby Emily1

Affiliation:

1. Centre of Genomics and Policy, School of Biomedical Sciences, Faculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada; email: , ,

2. Wellcome Sanger Institute, Hinxton, United Kingdom;

Abstract

The Human Cell Atlas (HCA) is striving to build an open community that is inclusive of all researchers adhering to its principles and as open as possible with respect to data access and use. However, open data sharing can pose certain challenges. For instance, being a global initiative, the HCA must contend with a patchwork of local and regional privacy rules. A notable example is the implementation of the European Union General Data Protection Regulation (GDPR), which caused some concern in the biomedical and genomic data-sharing community. We examine how the HCA's large, international group of researchers is investing tremendous efforts into ensuring appropriate sharing of data. We describe the HCA's objectives and governance, how it defines open data sharing, and ethico-legal challenges encountered early in its development; in particular, we describe the challenges prompted by the GDPR. Finally, we broaden the discussion to address tools and strategies that can be used to address ethical data governance.

Publisher

Annual Reviews

Subject

Genetics (clinical),Genetics,Molecular Biology

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