Toward a roadmap in global biobanking for health

Jennifer R. Harris*, Paul Burton, Bartha Maria Knoppers, Klaus Lindpaintner, Marianna Bledsoe, Anthony J. Brookes, Isabelle Budin-Ljosne, Rex Chisholm, David Cox, Mylène Deschênes, Isabel Fortier, Pierre Hainaut, Robert Hewitt, Jane Kaye, Jan Eric Litton, Andres Metspalu, Bill Ollier, Lyle J. Palmer, Aarno Palotie, Markus PasterkMarkus Perola, Peter H.J. Riegman, Gert Jan Van Ommen, Martin Yuille, Kurt Zatloukal

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

99 Scopus citations

Abstract

Biobanks can have a pivotal role in elucidating disease etiology, translation, and advancing public health. However, meeting these challenges hinges on a critical shift in the way science is conducted and requires biobank harmonization. There is growing recognition that a common strategy is imperative to develop biobanking globally and effectively. To help guide this strategy, we articulate key principles, goals, and priorities underpinning a roadmap for global biobanking to accelerate health science, patient care, and public health. The need to manage and share very large amounts of data has driven innovations on many fronts. Although technological solutions are allowing biobanks to reach new levels of integration, increasingly powerful data-collection tools, analytical techniques, and the results they generate raise new ethical and legal issues and challenges, necessitating a reconsideration of previous policies, practices, and ethical norms. These manifold advances and the investments that support them are also fueling opportunities for biobanks to ultimately become integral parts of health-care systems in many countries. International harmonization to increase interoperability and sustainability are two strategic priorities for biobanking. Tackling these issues requires an environment favorably inclined toward scientific funding and equipped to address socio-ethical challenges. Cooperation and collaboration must extend beyond systems to enable the exchange of data and samples to strategic alliances between many organizations, including governmental bodies, funding agencies, public and private science enterprises, and other stakeholders, including patients. A common vision is required and we articulate the essential basis of such a vision herein.

Original languageEnglish (US)
Pages (from-to)1105-1111
Number of pages7
JournalEuropean Journal of Human Genetics
Volume20
Issue number11
DOIs
StatePublished - Nov 2012

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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