The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2014-12-24

AUTHORS

Marina Mora, Corrado Angelini, Fabrizia Bignami, Anne-Mary Bodin, Marco Crimi, Jeanne- Hélène Di Donato, Alex Felice, Cécile Jaeger, Veronika Karcagi, Yann LeCam, Stephen Lynn, Marija Meznaric, Maurizio Moggio, Lucia Monaco, Luisa Politano, Manuel Posada de la Paz, Safaa Saker, Peter Schneiderat, Monica Ensini, Barbara Garavaglia, David Gurwitz, Diana Johnson, Francesco Muntoni, Jack Puymirat, Mojgan Reza, Thomas Voit, Chiara Baldo, Franca Dagna Bricarelli, Stefano Goldwurm, Giuseppe Merla, Elena Pegoraro, Alessandra Renieri, Kurt Zatloukal, Mirella Filocamo, Hanns Lochmüller

ABSTRACT

The EuroBioBank (EBB) network (www.eurobiobank.org) is the first operating network of biobanks in Europe to provide human DNA, cell and tissue samples as a service to the scientific community conducting research on rare diseases (RDs). The EBB was established in 2001 to facilitate access to RD biospecimens and associated data; it obtained funding from the European Commission in 2002 (5th framework programme) and started operation in 2003. The set-up phase, during the EC funding period 2003–2006, established the basis for running the network; the following consolidation phase has seen the growth of the network through the joining of new partners, better network cohesion, improved coordination of activities, and the development of a quality-control system. During this phase the network participated in the EC-funded TREAT-NMD programme and was involved in planning of the European Biobanking and Biomolecular Resources Research Infrastructure. Recently, EBB became a partner of RD-Connect, an FP7 EU programme aimed at linking RD biobanks, registries, and bioinformatics data. Within RD-Connect, EBB contributes expertise, promotes high professional standards, and best practices in RD biobanking, is implementing integration with RD patient registries and ‘omics’ data, thus challenging the fragmentation of international cooperation on the field. More... »

PAGES

1116-1123

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  • Journal

    TITLE

    European Journal of Human Genetics

    ISSUE

    9

    VOLUME

    23

    Author Affiliations

  • Muscle Cell Biology Lab, Neuromuscular Diseases and Neuroimmunolgy Unit, Fondazione Istituto Neurologico C. Besta, Milano, Italy
  • Department of Neurosciences, NPSRR University of Padova, Padova, Italy
  • GlaxoSmithKline, London, UK
  • EURORDIS, European Organisation for Rare Diseases, Paris, France
  • Fondazione Telethon, Milan, Italy
  • 3 C-R, Castelginest, France
  • Laboratory of Molecular Genetics and Malta BioBank, University of Malta, and Thalassaemia Clinic, Mater Dei Hospital, Msida, Malta
  • Hôpital Foch, Suresnes, France
  • Department of Molecular Genetics and Diagnostics, National Institute of Environmental Health, Budapest, Hungary
  • MRC Centre for Neuromuscular Diseases, Institute of Genetic Medicine, Newcastle University, International Centre for Life, Newcastle upon Tyne, UK
  • Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia
  • Neuromuscular Unit, IRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico, Dino Ferrari Centre, University of Milan, Milan, Italy
  • Division of Cardiomyology and Medical Genetics, Department of Experimental Medicine, Second University of Naples, Naples, Italy
  • Manuel Posada de la Paz, Institute of Rare Diseases Research, IIER, ISCIII and Spain RDR & CIBERER, Madrid, Spain
  • GENETHON, DNA and Cell Bank, Evry, France
  • Neurological Department, Muscle Tissue Culture Collection, Friedrich-Baur-Institute, Ludwig-Maximilians-University of Munich, Munich, Germany
  • Molecular Neurogenetics Unit, Fondazione Istituto Neurologico C. Besta, Milano, Italy
  • Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel
  • Dubowitz Neuromuscular Centre, MRC Neuromuscular Centre at UCL Institute of Child Health, London, UK
  • Department of Human Genetics, Centre Hospitalier Universitaire de Quebec, Quebec City, Quebec, Canada
  • Inserm U974—Institute of Myology, University Pierre and Marie Curie Paris 6, Paris, France
  • Laboratorio di Genetica Umana, E.O. Ospedali Galliera, Genova, Italy
  • Dipartimento Ligure di Genetica, E.O. Ospedali Galliera, Genova, Italy
  • Parkinson Institute, Istituti Clinici di Perfezionamento, Milano, Italy
  • Medical Genetics Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy
  • Division of Medical Genetics, University of Siena, Azienda Ospedaliera Universitaria Senese, Siena, Italy
  • Institute of Pathology, Medical University of Graz, Graz, Austria
  • Centro di Diagnostica Genetica e Biochimica delle Malattie Metaboliche, Istituto G. Gaslini, Genova, Italy
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/ejhg.2014.272

    DOI

    http://dx.doi.org/10.1038/ejhg.2014.272

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1007450136

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/25537360


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