Evidence map›Paper›PMID 41198707›Full record

ArticleScientific reports2025

Probing omics data via harmonic persistent homology.

Davide Gurnari, Aldo Guzmán-Sáenz, Filippo Utro, Aritra Bose, Saugata Basu, Laxmi Parida

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Davide Gurnari *Dioscuri Centre in Topological Data Analysis, Mathematical Institute PAN, Warsaw, Poland.ORCID http://orcid.org/0000-0002-3668-8711
Aldo Guzmán-Sáenz *IBM Research, Yorktown Heights, NY, USA.ORCID http://orcid.org/0000-0003-2725-621X
Filippo UtroIBM Research, Yorktown Heights, NY, USA.ORCID http://orcid.org/0000-0003-3226-7642
Aritra BoseIBM Research, Yorktown Heights, NY, USA.ORCID http://orcid.org/0000-0002-8665-056X
Saugata BasuDepartment of Mathematics, Purdue University, West Lafayette, IN, USA.ORCID http://orcid.org/0000-0002-2441-0915
Laxmi ParidaIBM Research, Yorktown Heights, NY, USA. parida@us.ibm.com.ORCID http://orcid.org/0000-0002-7872-5074

Funding

National Science Foundation (NSF) CCF-2128702
6 · The paper itself

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.

Indexed as

Computational BiologyGenomicsNeoplasmsAlgorithmsHumansData analysisMulti-omicsPattern discoveryTopological data analysis

Identifiers

PMID41198707
PMCPMC12592485

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.