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Leveraging European infrastructures to access 1 million human genomes by 2022. / Saunders, Gary; Baudis, Michael; Becker, Regina; Beltran, Sergi; Béroud, Christophe; Birney, Ewan; Brooksbank, Cath; Brunak, Søren; Van den Bulcke, Marc; Drysdale, Rachel; Capella-Gutierrez, Salvador; Flicek, Paul; Florindi, Francesco; Goodhand, Peter; Gut, Ivo; Heringa, Jaap; Holub, Petr; Hooyberghs, Jef; Juty, Nick; Keane, Thomas M; Korbel, Jan O; Lappalainen, Ilkka; Leskosek, Brane; Matthijs, Gert; Mayrhofer, Michaela Th; Metspalu, Andres; Navarro, Arcadi; Newhouse, Steven; Nyrönen, Tommi; Page, Angela; Persson, Bengt; Palotie, Aarno; Parkinson, Helen; Rambla, Jordi; Salgado, David; Steinfelder, Erik; Swertz, Morris A; Valencia, Alfonso; Varma, Susheel; Blomberg, Niklas; Scollen, Serena.
In:
Nature Reviews. Genetics, Vol. 20, 2019, p. 693-701.
Research output: Contribution to journal › Review › Research › peer-review
Harvard
Saunders, G, Baudis, M, Becker, R, Beltran, S, Béroud, C, Birney, E, Brooksbank, C
, Brunak, S, Van den Bulcke, M, Drysdale, R, Capella-Gutierrez, S, Flicek, P, Florindi, F, Goodhand, P, Gut, I, Heringa, J, Holub, P, Hooyberghs, J, Juty, N, Keane, TM, Korbel, JO, Lappalainen, I, Leskosek, B, Matthijs, G, Mayrhofer, MT, Metspalu, A, Navarro, A, Newhouse, S, Nyrönen, T, Page, A, Persson, B, Palotie, A, Parkinson, H, Rambla, J, Salgado, D, Steinfelder, E, Swertz, MA, Valencia, A, Varma, S, Blomberg, N & Scollen, S 2019, '
Leveraging European infrastructures to access 1 million human genomes by 2022',
Nature Reviews. Genetics, vol. 20, pp. 693-701.
https://doi.org/10.1038/s41576-019-0156-9APA
Saunders, G., Baudis, M., Becker, R., Beltran, S., Béroud, C., Birney, E., Brooksbank, C.
, Brunak, S., Van den Bulcke, M., Drysdale, R., Capella-Gutierrez, S., Flicek, P., Florindi, F., Goodhand, P., Gut, I., Heringa, J., Holub, P., Hooyberghs, J., Juty, N., ... Scollen, S. (2019).
Leveraging European infrastructures to access 1 million human genomes by 2022.
Nature Reviews. Genetics,
20, 693-701.
https://doi.org/10.1038/s41576-019-0156-9Vancouver
Saunders G, Baudis M, Becker R, Beltran S, Béroud C, Birney E et al.
Leveraging European infrastructures to access 1 million human genomes by 2022.
Nature Reviews. Genetics. 2019;20:693-701.
https://doi.org/10.1038/s41576-019-0156-9Author
Saunders, Gary ; Baudis, Michael ; Becker, Regina ; Beltran, Sergi ; Béroud, Christophe ; Birney, Ewan ; Brooksbank, Cath ; Brunak, Søren ; Van den Bulcke, Marc ; Drysdale, Rachel ; Capella-Gutierrez, Salvador ; Flicek, Paul ; Florindi, Francesco ; Goodhand, Peter ; Gut, Ivo ; Heringa, Jaap ; Holub, Petr ; Hooyberghs, Jef ; Juty, Nick ; Keane, Thomas M ; Korbel, Jan O ; Lappalainen, Ilkka ; Leskosek, Brane ; Matthijs, Gert ; Mayrhofer, Michaela Th ; Metspalu, Andres ; Navarro, Arcadi ; Newhouse, Steven ; Nyrönen, Tommi ; Page, Angela ; Persson, Bengt ; Palotie, Aarno ; Parkinson, Helen ; Rambla, Jordi ; Salgado, David ; Steinfelder, Erik ; Swertz, Morris A ; Valencia, Alfonso ; Varma, Susheel ; Blomberg, Niklas ; Scollen, Serena. / Leveraging European infrastructures to access 1 million human genomes by 2022. In: Nature Reviews. Genetics. 2019 ; Vol. 20. pp. 693-701.
Bibtex
@article{f3d1d35b334e4bbaa9d0872e37c61d87,
title = "Leveraging European infrastructures to access 1 million human genomes by 2022",
abstract = "Human genomics is undergoing a step change from being a predominantly research-driven activity to one driven through health care as many countries in Europe now have nascent precision medicine programmes. To maximize the value of the genomic data generated, these data will need to be shared between institutions and across countries. In recognition of this challenge, 21 European countries recently signed a declaration to transnationally share data on at least 1 million human genomes by 2022. In this Roadmap, we identify the challenges of data sharing across borders and demonstrate that European research infrastructures are well-positioned to support the rapid implementation of widespread genomic data access.",
author = "Gary Saunders and Michael Baudis and Regina Becker and Sergi Beltran and Christophe B{\'e}roud and Ewan Birney and Cath Brooksbank and S{\o}ren Brunak and {Van den Bulcke}, Marc and Rachel Drysdale and Salvador Capella-Gutierrez and Paul Flicek and Francesco Florindi and Peter Goodhand and Ivo Gut and Jaap Heringa and Petr Holub and Jef Hooyberghs and Nick Juty and Keane, {Thomas M} and Korbel, {Jan O} and Ilkka Lappalainen and Brane Leskosek and Gert Matthijs and Mayrhofer, {Michaela Th} and Andres Metspalu and Arcadi Navarro and Steven Newhouse and Tommi Nyr{\"o}nen and Angela Page and Bengt Persson and Aarno Palotie and Helen Parkinson and Jordi Rambla and David Salgado and Erik Steinfelder and Swertz, {Morris A} and Alfonso Valencia and Susheel Varma and Niklas Blomberg and Serena Scollen",
note = "Correction: https://www.nature.com/articles/s41576-019-0178-3",
year = "2019",
doi = "10.1038/s41576-019-0156-9",
language = "English",
volume = "20",
pages = "693--701",
journal = "Nature Reviews. Genetics",
issn = "1471-0056",
publisher = "nature publishing group",
}
RIS
TY - JOUR
T1 - Leveraging European infrastructures to access 1 million human genomes by 2022
AU - Saunders, Gary
AU - Baudis, Michael
AU - Becker, Regina
AU - Beltran, Sergi
AU - Béroud, Christophe
AU - Birney, Ewan
AU - Brooksbank, Cath
AU - Brunak, Søren
AU - Van den Bulcke, Marc
AU - Drysdale, Rachel
AU - Capella-Gutierrez, Salvador
AU - Flicek, Paul
AU - Florindi, Francesco
AU - Goodhand, Peter
AU - Gut, Ivo
AU - Heringa, Jaap
AU - Holub, Petr
AU - Hooyberghs, Jef
AU - Juty, Nick
AU - Keane, Thomas M
AU - Korbel, Jan O
AU - Lappalainen, Ilkka
AU - Leskosek, Brane
AU - Matthijs, Gert
AU - Mayrhofer, Michaela Th
AU - Metspalu, Andres
AU - Navarro, Arcadi
AU - Newhouse, Steven
AU - Nyrönen, Tommi
AU - Page, Angela
AU - Persson, Bengt
AU - Palotie, Aarno
AU - Parkinson, Helen
AU - Rambla, Jordi
AU - Salgado, David
AU - Steinfelder, Erik
AU - Swertz, Morris A
AU - Valencia, Alfonso
AU - Varma, Susheel
AU - Blomberg, Niklas
AU - Scollen, Serena
N1 - Correction: https://www.nature.com/articles/s41576-019-0178-3
PY - 2019
Y1 - 2019
N2 - Human genomics is undergoing a step change from being a predominantly research-driven activity to one driven through health care as many countries in Europe now have nascent precision medicine programmes. To maximize the value of the genomic data generated, these data will need to be shared between institutions and across countries. In recognition of this challenge, 21 European countries recently signed a declaration to transnationally share data on at least 1 million human genomes by 2022. In this Roadmap, we identify the challenges of data sharing across borders and demonstrate that European research infrastructures are well-positioned to support the rapid implementation of widespread genomic data access.
AB - Human genomics is undergoing a step change from being a predominantly research-driven activity to one driven through health care as many countries in Europe now have nascent precision medicine programmes. To maximize the value of the genomic data generated, these data will need to be shared between institutions and across countries. In recognition of this challenge, 21 European countries recently signed a declaration to transnationally share data on at least 1 million human genomes by 2022. In this Roadmap, we identify the challenges of data sharing across borders and demonstrate that European research infrastructures are well-positioned to support the rapid implementation of widespread genomic data access.
U2 - 10.1038/s41576-019-0156-9
DO - 10.1038/s41576-019-0156-9
M3 - Review
C2 - 31455890
VL - 20
SP - 693
EP - 701
JO - Nature Reviews. Genetics
JF - Nature Reviews. Genetics
SN - 1471-0056
ER -
