Abstract
Research biobanks are well-organized resources developed for the purpose of collecting, processing, storing, and distributing biological samples, accompanied by associated relevant clinical data, to make them accessible to further scientific investigation. In order to be efficient and reliable, genetic biobanks must implement specific guidelines. The detailed protocols for each step of the biobanking process strictly depend on the type and the aims of particular institution. However, some general policies should be followed, regarding key components of the banking process: obtaining informed initial consent to participate, proper collection of biological material, handling and transport of samples, freezing, storage, and retrieval of collected tissue as well as collection, protection, and sharing of relevant data.
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Further Reading
Hewitt RE (2011) Biobanking: the foundation of personalized medicine. Curr Opin Oncol 23:112–119
International Society for Biological and Environmental Repositories (ISBER) (2008) Collection, storage, retrieval and distribution of biological materials for research. Cell Preserv Technol 6:3–58. doi:10.1089/cpt.2008.9997
Kauffmann F, Cambon-Thomsen A (2008) Tracing biological collections: between books and clinical trials. JAMA 299:2316–2318
Sak J, Pawlikowski J, Goniewicz M, Witt M (2012) Population biobanking in selected European countries and proposed model for a polish national DNA bank. J Appl Genetics (in press). doi 10.1007/s13353-012-0082-4
Végvári A, Welinder C, Lindberg H, Fehniger TE, Marko-Varga G (2011) Biobank resources for future patient care: developments, principles and concepts. J Clin Bioinforma 1:24. doi:10.1186/2043-9113-1-24
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Poluha, A., Urbanowska, E. (2012). Biobanking of Cellular Material. In: Witt, M., Dawidowska, M., Szczepanski, T. (eds) Molecular Aspects of Hematologic Malignancies. Principles and Practice. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-29467-9_18
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DOI: https://doi.org/10.1007/978-3-642-29467-9_18
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