An efficient stochastic search for Bayesian variable selection with high-dimensional correlated predictors

  • Authors:
  • Deukwoo Kwon;Maria Teresa Landi;Marina Vannucci;Haleem J. Issaq;DaRue Prieto;Ruth M. Pfeiffer

  • Affiliations:
  • Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20852, USA;Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20852, USA;Department of Statistics, Rice University, Houston, TX 77251, USA;Lab of Proteomics and Analytical Technologies, SAIC-Frederick, Inc., Frederick, MD 21702, USA;Lab of Proteomics and Analytical Technologies, SAIC-Frederick, Inc., Frederick, MD 21702, USA;Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, MD 20852, USA

  • Venue:
  • Computational Statistics & Data Analysis
  • Year:
  • 2011

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Abstract

We present a Bayesian variable selection method for the setting in which the number of independent variables or predictors in a particular dataset is much larger than the available sample size. While most of the existing methods allow some degree of correlations among predictors but do not consider these correlations for variable selection, our method accounts for correlations among the predictors in variable selection. Our correlation-based stochastic search (CBS) method, the hybrid-CBS algorithm, extends a popular search algorithm for high-dimensional data, the stochastic search variable selection (SSVS) method. Similar to SSVS, we search the space of all possible models using variable addition, deletion or swap moves. However, our moves through the model space are designed to accommodate correlations among the variables. We describe our approach for continuous, binary, ordinal, and count outcome data. The impact of choices of prior distributions and hyperparameters is assessed in simulation studies. We also examined the performance of variable selection and prediction as the correlation structure of the predictors varies. We found that the hybrid-CBS resulted in lower prediction errors and identified better the true outcome associated predictors than SSVS when predictors were moderately to highly correlated. We illustrate the method on data from a proteomic profiling study of melanoma, a type of skin cancer.