Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jens-S Vöckler"'
Autor:
Veronica Wendy Setiawan, Jeffrey Haessler, Fredrick Schumacher, Michele L Cote, Ewa Deelman, Megan D Fesinmeyer, Brian E Henderson, Rebecca D Jackson, Jens-S Vöckler, Lynne R Wilkens, Shagufta Yasmeen, Christopher A Haiman, Ulrike Peters, Loïc Le Marchand, Charles Kooperberg
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30390 (2012)
We examined the association between HNF1B variants identified in a recent genome-wide association study and endometrial cancer in two large case-control studies nested in prospective cohorts: the Multiethnic Cohort Study (MEC) and the Women's Health
Externí odkaz:
https://doaj.org/article/5bdf54c8c3b040f08cfe9297481e716a
Scientists have a number of computing infrastructures available to conduct their research, including grids and public or private clouds. This paper explores the use of these cyberinfrastructures to execute scientific workflows, an important class of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcceafce89f5436e8f4c73b2cfb48d95
https://resolver.caltech.edu/CaltechAUTHORS:20130912-154730242
https://resolver.caltech.edu/CaltechAUTHORS:20130912-154730242
Autor:
Fredrick R. Schumacher, Charles Kooperberg, Christopher A. Haiman, Loic Le Marchand, Michele L. Cote, Rebecca D. Jackson, Megan D. Fesinmeyer, Shagufta Yasmeen, Ewa Deelman, Brian E. Henderson, Jens-S. Vöckler, Veronica Wendy Setiawan, Lynne R. Wilkens, Jeffrey Haessler, Ulrike Peters
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30390 (2012)
PLoS ONE
PLoS ONE
We examined the association between HNF1B variants identified in a recent genome-wide association study and endometrial cancer in two large case-control studies nested in prospective cohorts: the Multiethnic Cohort Study (MEC) and the Women's Health
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93256252f2873a70ac782d8215e8dc18
http://europepmc.org/articles/PMC3267708?pdf=render
http://europepmc.org/articles/PMC3267708?pdf=render
Autor:
Nancy S. Jenny, Charles B. Eaton, Petra Bůžková, Bruce M. Psaty, Charles Kooperberg, Danyu Lin, Lyle G. Best, Gerardo Heiss, Ewa Deelman, Eric Boerwinkle, Darin Taverna, Jens-S. Vöckler, Shelley A. Cole, Lucia A. Hindorff, Jonathan N. Bella, Nora Franceschini, Kari E. North, Philip Greenland, Ebony Bookman, Yi Lin, Alicia M. Young, Alexander P. Reiner, Tiana A. Garrett, Cara L. Carty
Background— Genome-wide association studies identified several single nucleotide polymorphisms (SNP) associated with prevalent coronary heart disease (CHD), but less is known of associations with incident CHD. The association of 13 published CHD SN
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c135a66acf3cc44ba68f8a2df54ee5bb
Publikováno v:
Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences. 371:20120066
The current model of transferring data from data centres to desktops for analysis will soon be rendered impractical by the accelerating growth in the volume of science datasets. Processing will instead often take place on high-performance servers co-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d59999319b9d9e2e4e9824e8704cbc0
https://doi.org/10.1098/rsta.2012.0066
https://doi.org/10.1098/rsta.2012.0066