论文概要 (Paper Overview)
Field: Machine Learning Authors: Kia Kazemi-Nia, Harsh Bandhey, Philip J. Freda, Ryan J. Urbanowicz Published: 2026-08-28 arXiv: 2608.28552
Abstract
As a precursor to high-dimensional biomedical data modeling, reliable feature selection can reduce computational expense, improve modeling performance, and yield simpler, more interpretable models. However, most filter-based feature selection methods struggle to detect feature interactions, while wrapper or embedded feature selection methods are computationally expensive. Relief-based algorithms (RBAs) are filter methods that are sensitive to feature interactions while mitigating these other limitations.
This study (1) refactors, optimizes, and expands the scikit-rebate Python package with existing and newly proposed RBA variants, and (2) conducts rigorous RBA benchmark comparisons across diverse genomic simulations. The expanded scikit-rebate includes SWRF*, mu-Relief, and 5 novel RBA variants implementing alternative strategies for neighbor selection and feature scoring.
Key Findings
- All RBAs were evaluated on simulated genomic datasets varying in sample size, feature count, heritability, and underlying association type (main effects and interactions), comparing predictive feature rankings and runtime.
- Except for mu-Relief, all RBAs excelled at detecting 2-way interactions in noisy data.
- RBAs using 'far' scoring were best at detecting 2-way interactions — MultiSWRFDB* performed best — but were considerably less sensitive to main effects.
- SWRF, MultiSWRF, MultiSURF, and MultiSWRFDB performed best on datasets with main effects and 2-way interactions; MultiSWRFDB was best when 3-way interactions were also considered.
- The refactoring of scikit-rebate reduced RBA runtimes by 10 to 35 times.
- The newly introduced RBAs are among the strongest performers, robustly preserving main effects and 2-way epistatic (interacting) signals for downstream modeling.
Conclusion
The refactored and expanded scikit-rebate package offers faster, interaction-sensitive filter-based feature selection. The new RBA variants balance detection of main effects and 2-way epistatic interactions, preserving predictive signal for downstream modeling of high-dimensional biomedical (genomic) data.
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