Probing omics data via harmonic persistent homology

Identifying molecular signatures from complex disease patients with underlying symptomatic similarities is a significant challenge in the analysis of high-dimensional multi-omics data. Topological data analysis (TDA) provides a way of extracting such information from the geometric structure of the data and identifying multi-way higher-order relationships. Here, we propose an application of harmonic persistent homology, which overcomes the limitation of the ambiguity of the choice of a cycle representing a specific homology class. When applied to multi-omics data, this leads to the discovery of hidden patterns highlighting the relationships between different omic profiles, while allowing for common tasks in multi-omics analyses, such as disease subtyping, and most importantly biomarker identification for similar latent biological pathways that are associated with complex diseases. Our experiments on multiple cancer data show that harmonic persistent homology effectively dissects multi-omics data to identify biomarkers by detecting representative cycles predictive of disease subtypes.

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Publication Details

Journal
Scientific Reports
Published
2025-11-06
DOI
https://doi.org/10.1038/s41598-025-12189-y
Citations
1
Primary Topic
Topological and Geometric Data Analysis
Type
article
Field-Weighted Citation Impact
1.50

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article

Probing omics data via harmonic persistent homology

Laxmi Parida, Aritra Bose, Davide Gurnari, Saugata Basu et al.
1 citations
Scientific Reports
Topological and Geometric Data Analysis
1.50
article

Probing omics data via harmonic persistent homology

Laxmi Parida, Aritra Bose, Davide Gurnari, Saugata Basu, Filippo Utro, Aldo Guzmán-Sáenz
article en
1 citations

Abstract

Identifying molecular signatures from complex disease patients with underlying symptomatic similarities is a significant challenge in the analysis of high-dimensional multi-omics data. Topological data analysis (TDA) provides a way of extracting such information from the geometric structure of the data and identifying multi-way higher-order relationships. Here, we propose an application of harmonic persistent homology, which overcomes the limitation of the ambiguity of the choice of a cycle representing a specific homology class. When applied to multi-omics data, this leads to the discovery of hidden patterns highlighting the relationships between different omic profiles, while allowing for common tasks in multi-omics analyses, such as disease subtyping, and most importantly biomarker identification for similar latent biological pathways that are associated with complex diseases. Our experiments on multiple cancer data show that harmonic persistent homology effectively dissects multi-omics data to identify biomarkers by detecting representative cycles predictive of disease subtypes.

Scientific ReportsVol. 15(1)
IBM (United States) (US), Purdue University West Lafayette (US)
National Science Foundation
Openalex Percentile: Top 12%
Topological and Geometric Data Analysis
1.50
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Probing omics data via harmonic persistent homology — Laxmi Parida, Aritra Bose, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS