Evidence map›Paper›PMID 40123934›Full record

ArticleIEEE access : practical innovations, open solutions2025

Comparative Analysis of Multi-Omics Integration Using Graph Neural Networks for Cancer Classification.

Fadi Alharbi, Aleksandar Vakanski, Boyu Zhang, Murtada K Elbashir, Mohanad Mohammed

Abstract read
In one paragraph

Article in IEEE access : practical innovations, open solutions, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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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

5 authors.

Fadi AlharbiCollege of Engineering, Department of Computer Science, University of Idaho, Moscow, ID 83844, USA.ORCID 0009-0005-1126-4356
Aleksandar VakanskiCollege of Engineering, Department of Computer Science, University of Idaho, Moscow, ID 83844, USA.ORCID 0000-0003-3365-1291
Boyu ZhangCollege of Engineering, Department of Computer Science, University of Idaho, Moscow, ID 83844, USA.ORCID 0000-0002-9401-6163
Murtada K ElbashirCollege of Computer and Information Sciences, Department of Information Systems, Jouf University, Sakaka, Al-Jouf 72441, Saudi Arabia.ORCID 0000-0003-3431-6604
Mohanad MohammedSchool of Mathematics, Statistics and Computer Science, University of KwaZulu-Natal, Pietermaritzburg 3209, South Africa.

Funding

Sequence-structure-function relationships in human visual photopigmentsP20GM104420 · NIGMS · UNIVERSITY OF IDAHO · PI MILLER, CRAIG R · 2015 to 2024
$22.9M
NIGMS NIH HHS P20 GM104420
6 · The paper itself

Abstract

Recent studies on integrating multiple omics data highlighted the potential to advance our understanding of the cancer disease process. Computational models based on graph neural networks and attention-based architectures have demonstrated promising results for cancer classification due to their ability to model complex relationships among biological entities. However, challenges related to addressing the high dimensionality and complexity in integrating multi-omics data, as well as in constructing graph structures that effectively capture the interactions between nodes, remain active areas of research. This study evaluates graph neural network architectures for multi-omics (MO) data integration based on graph-convolutional networks (GCN), graph-attention networks (GAT), and graph-transformer networks (GTN). Differential gene expression and LASSO (Least Absolute Shrinkage and Selection Operator) regression are employed for reducing the omics data dimensionality and feature selection; hence, the developed models are referred to as LASSO-MOGCN, LASSO-MOGAT, and LASSO-MOGTN. Graph structures constructed using sample correlation matrices and protein-protein interaction networks are investigated. Experimental validation is performed with a dataset of 8,464 samples from 31 cancer types and normal tissue, comprising messenger-RNA, micro-RNA, and DNA methylation data. The results show that the models integrating multi-omics data outperformed the models trained on single omics data, where LASSO-MOGAT achieved the best overall performance, with an accuracy of 95.9%. The findings also suggest that correlation-based graph structures enhance the models' ability to identify shared cancer-specific signatures across patients in comparison to protein-protein interaction networks-based graph structures. The code and data used in this study are available in the link (https://github.com/FadiAlharbi2024/Graph_Based_Architecture.git).

Indexed as

Cancer classificationcorrelation matricesgene expression analysisgraph neural networksmulti-omics data integrationprotein-protein interaction networks

Identifiers

PMID40123934
PMCPMC11928009

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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.