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A powerful penalized multinomial logistic regression approach.

Cornelia Fuetterer1, Malte Nalenz2, Thomas Augustin2

  • 1Institute of AI and Informatics in Medicine, School of Medicine and Health, TUM University Hospital, Technical University of Munich (TUM), Ismaninger Straße 22, 81675 Munich, Germany.

Computational Statistics
|October 27, 2025
PubMed
Summary
This summary is machine-generated.

We introduce discriminative power lasso (DP-lasso), a novel penalized regression method for categorical outcomes. DP-lasso effectively selects important predictors in high-dimensional settings, outperforming existing methods in simulations.

Keywords:
ClusteringPenalized regressionPenalty weightsPolytomous logistic regressionShrinkageSingle-cell RNA sequencing dataVariable selection

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Area of Science:

  • Statistics
  • Machine Learning
  • Bioinformatics

Background:

  • Penalized regression methods are crucial for prediction and variable selection in high-dimensional data.
  • Existing methods may struggle with correlated predictors and complex categorical outcomes.
  • There is a need for robust regularization techniques that balance prediction accuracy and interpretability.

Purpose of the Study:

  • To propose a novel penalized regression approach, discriminative power lasso (DP-lasso), for multinomial logistic models.
  • To incorporate predictor-specific weights based on intra- and inter-outcome category distances.
  • To evaluate DP-lasso's performance against existing methods in various simulation settings.

Main Methods:

  • Developed DP-lasso with an adaptive L1-type penalty term.
  • Proposed three measures for weight calculation: ANOVA-based and two clustering indices.
  • Conducted simulations with varying numbers of categories, predictors, association strengths, and correlations.

Main Results:

  • DP-lasso with ANOVA-based weights (DPan) produced sparser models, especially with correlated predictors in high-dimensional settings.
  • DPan demonstrated superior true positive rates and low false positive rates when the number of predictors (p) exceeded sample size (N).
  • DPan consistently achieved high true positive rates and the lowest false positive rates across all simulation scenarios, including when p < N.

Conclusions:

  • DPan is a highly recommended method for analyzing categorical outcomes with high-dimensional predictors.
  • The approach effectively handles correlated predictors and improves variable selection accuracy.
  • Demonstrated utility in ultra high-dimensional settings using single-cell RNA-sequencing data.