Literature DB >> 23990355

Variable selection in semi-parametric models.

Hongmei Zhang1, Arnab Maity2, Hasan Arshad3, John Holloway4, Wilfried Karmaus5.   

Abstract

We propose Bayesian variable selection methods in semi-parametric models in the framework of partially linear Gaussian and problit regressions. Reproducing kernels are utilized to evaluate possibly non-linear joint effect of a set of variables. Indicator variables are introduced into the reproducing kernels for the inclusion or exclusion of a variable. Different scenarios based on posterior probabilities of including a variable are proposed to select important variables. Simulations are used to demonstrate and evaluate the methods. It was found that the proposed methods can efficiently select the correct variables regardless of the feature of the effects, linear or non-linear in an unknown form. The proposed methods are applied to two real data sets to identify cytosine phosphate guanine methylation sites associated with maternal smoking and cytosine phosphate guanine sites associated with cotinine levels with creatinine levels adjusted. The selected methylation sites have the potential to advance our understanding of the underlying mechanism for the impact of smoking exposure on health outcomes, and consequently benefit medical research in disease intervention.
© The Author(s) 2013.

Entities:  

Keywords:  Bayesian methods; Gaussian kernel; non-linear effects; partially linear regression; probit regression; reproducing kernel; variable selection

Mesh:

Substances:

Year:  2013        PMID: 23990355      PMCID: PMC3938559          DOI: 10.1177/0962280213499679

Source DB:  PubMed          Journal:  Stat Methods Med Res        ISSN: 0962-2802            Impact factor:   3.021


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10.  450K epigenome-wide scan identifies differential DNA methylation in newborns related to maternal smoking during pregnancy.

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  4 in total

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3.  Cohort Profile: The Isle Of Wight Whole Population Birth Cohort (IOWBC).

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4.  DNA methylation loci associated with atopy and high serum IgE: a genome-wide application of recursive Random Forest feature selection.

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