Abstract:
:This paper is about an algorithm, FlexTree, for general supervised learning. It extends the binary tree-structured approach (Classification and Regression Trees, CART) although it differs greatly in its selection and combination of predictors. It is particularly applicable to assessing interactions: gene by gene and gene by environment as they bear on complex disease. One model for predisposition to complex disease involves many genes. Of them, most are pure noise; each of the values that is not the prevalent genotype for the minority of genes that contribute to the signal carries a "score." Scores add. Individuals with scores above an unknown threshold are predisposed to the disease. For the additive score problem and simulated data, FlexTree has cross-validated risk better than many cutting-edge technologies to which it was compared when small fractions of candidate genes carry the signal. For the model where only a precise list of aberrant genotypes is predisposing, there is not a systematic pattern of absolute superiority; however, overall, FlexTree seems better than the other technologies. We tried the algorithm on data from 563 Chinese women, 206 hypotensive, 357 hypertensive, with information on ethnicity, menopausal status, insulin-resistant status, and 21 loci. FlexTree and Logic Regression appear better than the others in terms of Bayes risk. However, the differences are not significant in the usual statistical sense.
journal_name
Proc Natl Acad Sci U S Aauthors
Huang J,Lin A,Narasimhan B,Quertermous T,Hsiung CA,Ho LT,Grove JS,Olivier M,Ranade K,Risch NJ,Olshen RAdoi
10.1073/pnas.0403794101keywords:
subject
Has Abstractpub_date
2004-07-20 00:00:00pages
10529-34issue
29eissn
0027-8424issn
1091-6490pii
0403794101journal_volume
101pub_type
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