Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities. (2012)
Attributed to:
Identification of copy number variants in familial and pathologically proven PD
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.22161
PubMed Identifier: 22777693
Publication URI: http://europepmc.org/abstract/MED/22777693
Type: Journal Article/Review
Volume: 33
Parent Publication: Human mutation
Issue: 12
ISSN: 1059-7794