OMIDIENT: Multiomics Integration for Cancer by Dirichlet Auto-Encoder Networks
5 affiliations
- 1Dept. of Computer Science, Aalto University, Helsinki, Finland
- 2Dept. of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland
- 3Applied Tumor Genomics Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland
- 4Mohamed bin Zayed University of Artificial Intelligence, Abu Dhabi, UAE
- 5iCAN Digital Precision Cancer Medicine Flagship, University of Helsinki, Helsinki, Finland
Abstract
To achieve a more comprehensive understanding of cancer, novel computational methods are required for the integrative analysis of data from different molecular layers, such as genomics, transcriptomics, and epigenomics. Here, we present an innovative multi-omics integrative method that performs unsupervised representation learning, referred to as OMIDIENT: multiOMics Integration for cancer by DIrichlet auto-ENcoder neTworks. OMIDIENT provides a natural framework for modeling sparse and compositional latent representations by employing a deep generative model, where the latent space is distributed as the product of Dirichlet distributions. Applied to five different cancers, we demonstrate that OMIDIENT outperforms the top state-of-the-art unsupervised multi-omics integrative analysis approaches in clustering, classification, and reconstruction of missing data using mRNA expression data, DNA methylation data, and microRNA expression data. Furthermore, we provide interpretability analyses for OMIDIENT that not only support its improved performance, but also offer valuable insights into the underlying structure captured by the learned representations.
Related
- Multi-Omic Integration of the miRNome and Transcriptome in Dermal Fibroblasts from Hypermobile Ehlers–Danlos Syndrome and Hypermobility Spectrum Disorders Identifies Convergent Candidate miRNA-mRNA Regulatory Networks Linking Extracellular Matrix Remodeling and Inflammation
- Decomposing multi-scale dynamic regulation from single-cell multiomics with scMagnify
- A generalizable Hi-C foundation model for chromatin architecture, single-cell and multiomics analysis across species
- Multiomics analysis reveals the enhancer landscapes and 3D chromatin architecture in esophageal squamous cell carcinoma
- Roadmap for inferring metabolic regulation using multiomics, machine learning, and genome-scale modeling.
BibTeX
@article{safinianaini2026omidient,
title = {{OMIDIENT: Multiomics Integration for Cancer by Dirichlet Auto-Encoder Networks}},
author = {Negar Safinianaini and Niko Välimäki and Roman Bresson and Alexandra Gorbonos and Kristiina Rajamäki and Lauri A. Aaltonen and Pekka Marttinen},
journal = {Communications Biology},
year = {2026},
month = jul,
doi = {10.1038/s42003-026-10578-1},
url = {https://doi.org/10.1038/s42003-026-10578-1},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - OMIDIENT: Multiomics Integration for Cancer by Dirichlet Auto-Encoder Networks
AU - Negar Safinianaini
AU - Niko Välimäki
AU - Roman Bresson
AU - Alexandra Gorbonos
AU - Kristiina Rajamäki
AU - Lauri A. Aaltonen
AU - Pekka Marttinen
PY - 2026
DA - 2026/07/06
JO - Communications Biology
DO - 10.1038/s42003-026-10578-1
UR - https://doi.org/10.1038/s42003-026-10578-1
AB - To achieve a more comprehensive understanding of cancer, novel computational methods are required for the integrative analysis of data from different molecular layers, such as genomics, transcriptomics, and epigenomics. Here, we present an innovative multi-omics integrative method that performs unsupervised representation learning, referred to as OMIDIENT: multiOMics Integration for cancer by DIrichlet auto-ENcoder neTworks. OMIDIENT provides a natural framework for modeling sparse and compositional latent representations by employing a deep generative model, where the latent space is distributed as the product of Dirichlet distributions. Applied to five different cancers, we demonstrate that OMIDIENT outperforms the top state-of-the-art unsupervised multi-omics integrative analysis approaches in clustering, classification, and reconstruction of missing data using mRNA expression data, DNA methylation data, and microRNA expression data. Furthermore, we provide interpretability analyses for OMIDIENT that not only support its improved performance, but also offer valuable insights into the underlying structure captured by the learned representations.
SN - 2399-3642
ER -