Making sense of big data in health research: Towards an EU action plan

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3085528 25 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Making sense of big data in health research: Towards an EU action plan
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Medicine and healthcare are undergoing profound changes. Whole-genome sequencing and high-resolution imaging technologies are key drivers of this rapid and crucial transformation. Technological innovation combined with automation and miniaturization has triggered an explosion in data production that will soon reach exabyte proportions. How are we going to deal with this exponential increase in data production? The potential of "big data" for improving health is enormous but, at the same time, we face a wide range of challenges to overcome urgently. Europe is very proud of its cultural diversity; however, exploitation of the data made available through advances in genomic medicine, imaging, and a wide range of mobile health applications or connected devices is hampered by numerous historical, technical, legal, and political barriers. European health systems and databases are diverse and fragmented. There is a lack of harmonization of data formats, processing, analysis, and data transfer, which leads to incompatibilities and lost opportunities. Legal frameworks for data sharing are evolving. Clinicians, researchers, and citizens need improved methods, tools, and training to generate, analyze, and query data effectively. Addressing these barriers will contribute to creating the European Single Market for health, which will improve health and healthcare for all Europeans. © 2016 The Author(s).
Έτος δημοσίευσης:
2016
Συγγραφείς:
Auffray, C.
Balling, R.
Barroso, I.
Bencze, L.
Benson, M.
Bergeron, J.
Bernal-Delgado, E.
Blomberg, N.
Bock, C.
Conesa, A.
Del Signore, S.
Delogne, C.
Devilee, P.
Di Meglio, A.
Eijkemans, M.
Flicek, P.
Graf, N.
Grimm, V.
Guchelaar, H.-J.
Guo, Y.-K.
Gut, I.G.
Hanbury, A.
Hanif, S.
Hilgers, R.-D.
Honrado
Hose, D.R.
Houwing-Duistermaat, J.
Hubbard, T.
Janacek, S.H.
Karanikas, H.
Kievits, T.
Kohler, M.
Kremer, A.
Lanfear, J.
Lengauer, T.
Maes, E.
Meert, T.
Müller, W.
Nickel, D.
Oledzki, P.
Pedersen, B.
Petkovic, M.
Pliakos, K.
Rattray, M.
i Màs, J.R.
Schneider, R.
Sengstag, T.
Serra-Picamal, X.
Spek, W.
Vaas, L.A.I.
van Batenburg, O.
Vandelaer, M.
Varnai, P.
Villoslada, P.
Vizcaíno, J.A.
Wubbe, J.P.M.
Zanetti, G.
Περιοδικό:
Genome Medicine
Εκδότης:
BioMed Central Ltd.
Τόμος:
8
Αριθμός / τεύχος:
1
Λέξεις-κλειδιά:
Article; data analysis; electronic health record; Europe; gene sequence; genetic database; genome analysis; government regulation; health care system; human; legal aspect; mathematical model; medical education; medical research; nonhuman; patient information; patient registry; priority journal; process model; register; sequence analysis; European Union; factual database; health care planning; information dissemination; legislation and jurisprudence; medical research; organization and management; standards, Biomedical Research; Databases, Factual; European Union; Health Plan Implementation; Humans; Information Dissemination
Επίσημο URL (Εκδότης):
DOI:
10.1186/s13073-016-0323-y
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