Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities. (2012)

First Author: Mittag F
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