Evidence map›Paper›PMID 42412838›Full record

ArticleBioinformatics (Oxford, England)2026

EPIC: Event Prototyping via Information Constrained graph learning for personalized cancer driver gene prediction.

Sang-Pil Cho, Young-Rae Cho

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. 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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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Sang-Pil ChoDepartment of Software, Yonsei University-Mirae Campus, Wonju-si, Gangwon-do, 26493, Republic of Korea.
Young-Rae ChoDepartment of Software, Yonsei University-Mirae Campus, Wonju-si, Gangwon-do, 26493, Republic of Korea.ORCID 0000-0002-4645-2542

Funding

Basic Science Research ProgramGangwon State,Republic of Korea 2026-RISE-10-006Ministry of EducationMinistry of Education RS-2025-25432919Ministry of Scienceand ICT RS-2025-16067916National Research Foundationof KoreaNRFRegional Innovation System & Education
6 · The paper itself

Abstract

motivationPrecision oncology relies on accurately distinguishing patient-specific driver mutations from the vast background of passenger alterations. While graph-based computational methods have emerged as powerful tools for this task, they often struggle to preserve the distinct genomic context of individual mutations within complex biological networks. Consequently, subtle patient-specific driver signals are frequently obscured by dominant topological patterns, critically impeding the identification of individualized oncogenic events essential for personalized cancer therapy.

resultsTo address this, we propose EPIC, a novel framework for Event Prototyping via Information Constrained Graph Learning. Unlike traditional node-centric approaches, EPIC redefines driver prediction as a metric learning task in an event embedding space. We introduce an information-constrained learning strategy that imposes explicit geometric constraints on feature variance, effectively preventing feature collapse and ensuring that low-frequency driver signals are distinctively preserved. Experiments on large-scale cancer cohorts demonstrate that EPIC significantly outperforms established baselines. Notably, the model prioritizes low-frequency driver variants typically overlooked by population-based methods, mapping them to critical oncogenic mechanisms associated with drug resistance and metastasis. Furthermore, clinical actionability analysis confirms that EPIC substantially expands the patient population eligible for targeted therapies. EPIC provides a robust and context-aware solution for personalized cancer driver discovery, bridging the gap between genomic data and actionable therapeutic insights. AVAILABILITY AND IMPLEMENTATION: The source code and datasets are available at https://github.com/spcho-dev/EPIC.

Indexed as

Computational BiologyNeoplasmsOncogenesPrecision MedicineSoftwareAlgorithmsHumansMachine LearningMutation

Identifiers

PMID42412838
PMCPMC13340217

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.