Aug 2026· PeerJ Computer Science· Vol 12, pp. e3298· 0 citations· 51 references
TL;DR
A novel cancer subtype classification framework using multi-omics integration and an ensemble-based parallel DL/ML architecture with multimodal autoencoder used for effective feature learning across omics types, overcoming the limitations of naïve concatenation is presented.
Abstract
Integrating multi-omics data to understand biological processes in human diseases is a complex bioinformatic task. Machine learning (ML), particularly deep learning (DL) models, offers a promising approach to multi-omics data integration and analysis. However, existing DL models generally integrate multi-omics data by concatenating the input data space or learned feature space, which is a sub-optimal approach. In addition, single classifiers are commonly used in DL-based methods, which can compromise the performance. Furthermore, the gradient descent optimization technique in DL suffers from a high computational cost and local sub-optimal solutions. To address these challenges, this article presents a novel cancer subtype classification framework using multi-omics integration and an ensemble-based parallel DL/ML architecture. Specifically, a multimodal autoencoder is used for effective feature learning across omics types, overcoming the limitations of naïve concatenation. A hybrid ensemble model comprising DL and ML learners with a meta-learner enhances classification robustness beyond single models. To improve optimization and computation, we incorporate a hybrid Back-Propagation and Particle Swarm Optimization (PSO) strategy and execute the entire framework on a parallel processing platform, reducing computation time while enhancing global search capability. The proposed framework is evaluated empirically with two benchmark data sets from The Cancer Genome Atlas (TCGA), namely the TCGA Pan-cancer and TCGA Breast Invasive Carcinoma (BRCA) data sets. The results indicate a high performance with accuracy rates of 89.51% and 90.9% for TCGA Pan-cancer and TCGA BRCA, respectively. The parallel implementation of the proposed framework reduces the computation time, resulting in a speed-up of 3 times and 2.5 times for TCGA Pan-cancer and TCGA BRCA, respectively. The findings ascertain the efficacy of the proposed framework for the classification of cancer subtypes, offering a promising solution for implementation in real-world environments.
A comprehensive analysis of data from multiple omics is essential for devising precise therapeutic strategies for complex diseases. The effective integration and analysis of multi-omic data can boost the precise classification of disease subtypes. However, existing methods for multi-omic data integration learning suf...
Yan-Mei Lin, Ya-Ting Zhong, Zhu-Hong You et al.· Scientific Reports· 0 citations
Cluster analysis showed the importance of well-defined clusters, indicating that while silhouette scores were linked to prediction success, biological variability also played a critical role, indicating that while silhouette scores were linked to prediction success, biological variability also played a critical role.
Sara Amjad, M. M. Sufyan Beg, Mohd. Azhar Aziz· Current Issues in Molecular...· 0 citations
The proposed TMO-Net+ improves the robustness and cross-cancer transferability of multi-omics representations within the evaluated TCGA cohorts, and offers a reliable framework for integrative tumor analysis within the evaluated TCGA cohorts.
Wei Liu, Xuan Liu, Shu-Yu Zhou et al.· Genes· 0 citations
This review highlights the potential of DL and multi-omics integration in advancing precision oncology for brain cancer by enhancing diagnostic precision, prognostic accuracy, and personalized therapy development.
Sana Munquad, Anam Upadhyay, A. Das· Frontiers in Bioinformatics· 0 citations
MOXAI (Multi-Omics Based Explainable AI), a deep learning framework that integrates DNA methylation and copy number data from methylation arrays to classify molecular subtypes of adult-type diffuse gliomas, is presented, alongside single-modality variants for comparison.
M. Alom, Quynh T. Tran, Breuer Alexandar et al.· 0 citations
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