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

First Author: Mittag F

Attributed to: ERANET 1 NEURON 3: 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