Evidence map›Paper›PMID 41133270›Full record

ArticleNAR genomics and bioinformatics2025

E-ABIN: an explainable module for anomaly detection in biological networks.

Ugo Lomoio, Tommaso Mazza, Pierangelo Veltri, Pietro Hiram Guzzi

Abstract read
In one paragraph

Article in NAR genomics and bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ugo LomoioDepartment of Surgical and Medical Sciences, Magna Graecia University, Viale Europa, 88100 Catanzaro, Italy.
Tommaso MazzaComputational Biology and Bioinformatics Unit, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Roma, Italy.
Pierangelo VeltriDIMES, University of Calabria, 87036 Rende, Italy.
Pietro Hiram GuzziDepartment of Surgical and Medical Sciences, Magna Graecia University, Viale Europa, 88100 Catanzaro, Italy.ORCID https://orcid.org/0000-0001-5542-2997

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing availability of large-scale omics data calls for robust analytical frameworks capable of handling complex gene expression datasets while offering interpretable results. Recent advances in artificial intelligence have enabled the identification of aberrant molecular patterns distinguishing disease states from healthy controls. Coupled with improvements in model interpretability, these tools now support the identification of genes potentially driving disease phenotypes. However, current approaches to gene anomaly detection often remain limited to single datasets and lack accessible graphical interfaces. We introduce E-ABIN, a general-purpose, explainable framework for anomaly detection in biological networks. E-ABIN combines classical machine learning and graph-based deep learning techniques within a unified, user-friendly platform, enabling the detection and interpretation of anomalies from gene expression or methylation-derived networks. By integrating algorithms such as support vector machines, random forests, graph autoencoders, and graph adversarial attributed networks, E-ABIN ensures high predictive accuracy while maintaining interpretability. We demonstrate the utility of E-ABIN through case studies of bladder cancer and celiac disease, where it effectively uncovers biologically relevant anomalies and offers insights into disease mechanisms. E-ABIN is freely available on the Zenodo platform at https://doi.org/10.5281/zenodo.17062501.

Indexed as

Celiac DiseaseComputational BiologyGene Regulatory NetworksSoftwareUrinary Bladder NeoplasmsAlgorithmsDeep LearningHumansMachine Learning

Identifiers

PMID41133270
PMCPMC12541387

What Socratic holds

Textmetadata
LicenceCC BY-NC
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Registered trials

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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 Socratic graph.