Use of support vector machines for disease risk prediction in genome-wide association studies: Concerns and opportunities
- Florian Mittag
- , Finja Büchel
- , Mohamad Saad
- , Andreas Jahn
- , Claudia Schulte
- , Zoltan Bochdanovits
- , Javier Simón-Sánchez
- , Mike A. Nalls
- , Margaux Keller
- , Dena G. Hernandez
- , J. Raphael Gibbs
- , Suzanne Lesage
- , Alexis Brice
- , Peter Heutink
- , Maria Martinez
- , Nicholas W. Wood
- , John Hardy
- , Andrew B. Singleton
- , Andreas Zell
- , Thomas Gasser
*Corresponding author for this work
- University of Tübingen
- Institut national de la santé et de la recherche médicale
- INSERM UMR 1043 and Paul Sabatier University
- German Center for Neurodegenerative Diseases
- VU University Medical Center
- National Institutes of Health
- Temple University
- University College London
- Sorbonne Université
- CNRS
Research output: Contribution to journal › Article › peer-review
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