Uncovering heterogeneous effects via localized feature selection

Identifying features that interact to trigger disease, while accounting for heterogeneity across diverse populations, is essential for the development of precision and targeted medicine. Despite the availability of vast and complex health-related datasets, most existing works focus on identifying disease-associated features at the population level or within a few subpopulations, often overlooking individual-level heterogeneity within these groups. To address this limitation, we propose a framework that utilizes localized test statistics to identify disease-associated features tailored to individual profiles. Our method leverages the recently developed knockoffs methodology to control the noise level of the selection set so that the results are replicable. Moreover, it allows for the discovery of hidden heterogeneous effects within the data, as demonstrated in an application to single-cell RNA sequencing data for Alzheimer’s disease. By aggregating localized feature selection results, our framework also enables powerful population-level feature selection. Our framework provides a powerful tool for exploratory studies of precision medicine, offering the potential to generate novel hypotheses for confirmatory biological experiments.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-09-15
DOI
https://doi.org/10.1073/pnas.2527033123
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

Uncovering heterogeneous effects via localized feature selection

Robert R. Butler, Zhaomeng Chen, Zihuai He, Jiaqi Gu et al.
Proceedings of the National Academy of Sciences
Single-cell and spatial transcriptomics
article

Uncovering heterogeneous effects via localized feature selection

Robert R. Butler, Zhaomeng Chen, Zihuai He, Jiaqi Gu, Iuliana Ionita‐Laza, Jinzhou Li, Linxi Liu, Tim Morrison, Hua Tang, Jacob Edelson, Emmanuel Candès, Benjamin Chu, Xiaoxia Liu, Chiara Sabatti, Frank M. Longo
article en

Abstract

Identifying features that interact to trigger disease, while accounting for heterogeneity across diverse populations, is essential for the development of precision and targeted medicine. Despite the availability of vast and complex health-related datasets, most existing works focus on identifying disease-associated features at the population level or within a few subpopulations, often overlooking individual-level heterogeneity within these groups. To address this limitation, we propose a framework that utilizes localized test statistics to identify disease-associated features tailored to individual profiles. Our method leverages the recently developed knockoffs methodology to control the noise level of the selection set so that the results are replicable. Moreover, it allows for the discovery of hidden heterogeneous effects within the data, as demonstrated in an application to single-cell RNA sequencing data for Alzheimer’s disease. By aggregating localized feature selection results, our framework also enables powerful population-level feature selection. Our framework provides a powerful tool for exploratory studies of precision medicine, offering the potential to generate novel hypotheses for confirmatory biological experiments.

Proceedings of the National Academy of SciencesVol. 123(38)
National University of Singapore (SG), University of Pittsburgh (US), University of South Florida (US), Quantitative BioSciences (US), Jacobs (United Kingdom) (GB), University at Buffalo, State University of New York (US), Columbia University (US), Stanford University (US)
Openalex Percentile: Top 18%
Single-cell and spatial transcriptomics
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