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Original Paper

Symbolic Modeling of Epistasis

Moore J.H.a-f · Barney N.a · Tsai C.-T.g · Chiang F.-T.g · Gui J.a, c · White B.C.a

Author affiliations

aComputational Genetics Laboratory, Departments of bGenetics and cCommunity and Family Medicine, Norris-Cotton Cancer Center, Dartmouth Medical School, Lebanon, N.H., dDepartment of Biological Sciences, Dartmouth College, Hanover, N.H., eDepartment of Computer Science, University of New Hampshire, Durham, N.H., fDepartment of Computer Science, University of Vermont, Burlington, Vt., USA; gDivision of Cardiology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

Related Articles for ""

Hum Hered 2007;63:120–133

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Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: July 16, 2006
Accepted: October 05, 2006
Published online: February 02, 2007
Issue release date: February 2007

Number of Print Pages: 14
Number of Figures: 5
Number of Tables: 2

ISSN: 0001-5652 (Print)
eISSN: 1423-0062 (Online)

For additional information: http://www.karger.com/HHE

Abstract

The workhorse of modern genetic analysis is the parametric linear model. The advantages of the linear modeling framework are many and include a mathematical understanding of the model fitting process and ease of interpretation. However, an important limitation is that linear models make assumptions about the nature of the data being modeled. This assumption may not be realistic for complex biological systems such as disease susceptibility where nonlinearities in the genotype to phenotype mapping relationship that result from epistasis, plastic reaction norms, locus heterogeneity, and phenocopy, for example, are the norm rather than the exception. We have previously developed a flexible modeling approach called symbolic discriminant analysis (SDA) that makes no assumptions about the patterns in the data. Rather, SDA lets the data dictate the size, shape, and complexity of a symbolic discriminant function that could include any set of mathematical functions from a list of candidates supplied by the user. Here, we outline a new five step process for symbolic model discovery that uses genetic programming (GP) for coarse-grained stochastic searching, experimental design for parameter optimization, graphical modeling for generating expert knowledge, and estimation of distribution algorithms for fine-grained stochastic searching. Finally, we introduce function mapping as a new method for interpreting symbolic discriminant functions. We show that function mapping when combined with measures of interaction information facilitates statistical interpretation by providing a graphical approach to decomposing complex models to highlight synergistic, redundant, and independent effects of polymorphisms and their composite functions. We illustrate this five step SDA modeling process with a real case-control dataset.

© 2007 S. Karger AG, Basel


Article / Publication Details

First-Page Preview
Abstract of Original Paper

Received: July 16, 2006
Accepted: October 05, 2006
Published online: February 02, 2007
Issue release date: February 2007

Number of Print Pages: 14
Number of Figures: 5
Number of Tables: 2

ISSN: 0001-5652 (Print)
eISSN: 1423-0062 (Online)

For additional information: http://www.karger.com/HHE


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