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Simultaneous inference for generalized linear models with unmeasured confounders.

Jin-Hong Du1,2, Larry Wasserman1,2, Kathryn Roeder1,3

  • 1Department of Statistics and Data Science, Carnegie Mellon University, Pittsburgh, PA 15213, USA.

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|September 18, 2025
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Summary
This summary is machine-generated.

This study introduces a new statistical framework to address bias in large-scale hypothesis testing for genomic studies caused by unmeasured confounding effects. The method effectively controls errors and improves power in identifying differentially expressed genes.

Keywords:
Hidden variablesHigh-dimensional regressionHypothesis testingMultivariate response regressionNuisance parametersSurrogate variables analysis

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Area of Science:

  • Genomics
  • Statistical Genetics
  • Bioinformatics

Background:

  • Genomic studies often involve tens of thousands of simultaneous hypothesis tests to identify differentially expressed genes.
  • Standard statistical approaches can be substantially biased due to unmeasured confounding effects.
  • Accurate statistical inference is crucial for reliable identification of gene expression differences.

Purpose of the Study:

  • To develop a unified statistical framework for large-scale hypothesis testing in multivariate generalized linear models with confounding effects.
  • To address the challenge of unmeasured confounders in genomic data analysis.
  • To improve the accuracy and power of identifying differentially expressed genes.

Main Methods:

  • A novel framework using orthogonal structures and linear projections is proposed.
  • The method disentangles confounding effects, jointly estimates latent factors and primary effects via lasso-type optimization.
  • Bias-correction steps are incorporated for hypothesis testing, with theoretical guarantees on identification and error bounds.

Main Results:

  • The proposed method demonstrates effective Type-I error control for asymptotic z-tests.
  • Numerical experiments show the method controls the false discovery rate and offers increased power compared to alternatives.
  • Application to single-cell RNA-seq data validates its suitability for adjusting confounding effects, even without explicit covariates.

Conclusions:

  • The developed statistical framework provides a robust solution for hypothesis testing in the presence of arbitrary confounding mechanisms.
  • The method enhances the reliability of findings in large-scale genomic studies.
  • It offers a practical approach for adjusting confounding effects in complex biological data.