Heterogeneity-preserving discriminative feature selection for disease-specific subtype discovery

Disease-specific subtype identification can deepen our understanding of disease progression and pave the way for personalized therapies, given the complexity of disease heterogeneity. Large-scale transcriptomic, proteomic, and imaging datasets create opportunities for discovering subtypes but also pose challenges due to their high dimensionality. To mitigate this, many feature selection methods focus on selecting features that distinguish known diseases or cell states, yet often miss features that preserve heterogeneity and reveal new subtypes. To overcome this gap, we develop Preserving Heterogeneity (PHet), a statistical methodology that employs iterative subsampling and differential analysis of interquartile range, in conjunction with Fisher's method, to identify a small set of features that enhance subtype clustering quality. Here, we show that this method can maintain sample heterogeneity while distinguishing known disease/cell states, with a tendency to outperform previous differential expression and outlier-based methods, indicating its potential to advance our understanding of disease mechanisms and cell differentiation.

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Publication Details

Journal
Nature Communications
Published
2025-04-15
DOI
https://doi.org/10.1038/s41467-025-58718-1
Citations
6
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
4.84

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article

Heterogeneity-preserving discriminative feature selection for disease-specific subtype discovery

Caleb Hallinan, Abdur Rahman M. A. Basher, Kwonmoo Lee
6 citations
Nature Communications
Gene expression and cancer classification
4.84
article

Heterogeneity-preserving discriminative feature selection for disease-specific subtype discovery

Caleb Hallinan, Abdur Rahman M. A. Basher, Kwonmoo Lee
article en
6 citations

Abstract

Disease-specific subtype identification can deepen our understanding of disease progression and pave the way for personalized therapies, given the complexity of disease heterogeneity. Large-scale transcriptomic, proteomic, and imaging datasets create opportunities for discovering subtypes but also pose challenges due to their high dimensionality. To mitigate this, many feature selection methods focus on selecting features that distinguish known diseases or cell states, yet often miss features that preserve heterogeneity and reveal new subtypes. To overcome this gap, we develop Preserving Heterogeneity (PHet), a statistical methodology that employs iterative subsampling and differential analysis of interquartile range, in conjunction with Fisher's method, to identify a small set of features that enhance subtype clustering quality. Here, we show that this method can maintain sample heterogeneity while distinguishing known disease/cell states, with a tendency to outperform previous differential expression and outlier-based methods, indicating its potential to advance our understanding of disease mechanisms and cell differentiation.

Nature CommunicationsVol. 16(1)
Boston Children's Hospital (US), Harvard University (US)
National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Reduced inequalities
Openalex Percentile: Top 5%
Gene expression and cancer classification
4.84
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