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Updated: Apr 29, 2026

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Bayesian analysis of high-dimensional gene expression using semiparametric quantile regression.

Taha Alshaybawee1, Saif Hosam Raheem1, Asaad Naser Hussein Mzedawee1,2

  • 1Department of Statistics, College of Administration and Economics, University of Al-Qadisiyah, Al Diwaniyah, Iraq.

Journal of Biopharmaceutical Statistics
|April 27, 2026
PubMed
Summary

This study introduces a new Bayesian Semiparametric Quantile Regression (BSQR) method for analyzing complex gene expression data. BSQR offers improved accuracy and gene selection compared to existing methods, especially in high-dimensional genomic studies.

Keywords:
Bayesian semiparametric quantile regressionGaussian process priorshigh-dimensional genomicsposterior inclusion probability (PIP)variable selection

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Area of Science:

  • Genomics
  • Statistical Genetics
  • Bioinformatics

Background:

  • High-dimensional gene expression data often presents challenges like heterogeneity, nonlinearities, and distributional shifts.
  • Traditional mean regression methods struggle to capture these complex patterns effectively.

Purpose of the Study:

  • To develop a novel Bayesian Semiparametric Quantile Regression (BSQR) framework.
  • To integrate Gaussian process priors for nonlinear modeling and sparsity-inducing priors for variable selection.
  • To enhance the analysis of high-dimensional genomic data by addressing its inherent complexities.

Main Methods:

  • The proposed BSQR framework utilizes Gaussian process priors for nonlinear modeling.
  • Sparsity-inducing priors are employed for effective variable selection.
  • Gene relevance is determined using posterior inclusion probabilities (PIPs) and effect size thresholds with false discovery control.

Main Results:

  • Extensive simulations demonstrate BSQR's superior performance over penalized B-spline quantile regression (B-SP).
  • BSQR shows enhanced precision, recall, probability calibration, and robustness under nonlinear and heteroskedastic conditions.
  • The method achieved higher AUCs, lower Brier scores, and more stable gene discovery across quantiles.

Conclusions:

  • BSQR offers a flexible and powerful approach for quantile-specific genomic analysis in high-dimensional settings.
  • Application to a breast cancer dataset confirmed BSQR's advantages in discrimination, calibration, and selection reliability.
  • The framework provides principled inference with false discovery control for genomic studies.