Abstract
Multi-omics promises to transform medicine by providing holistic disease insights through interacting molecular layers, involving DNA, RNA, proteins and metabolites. The underlying technologies have matured rapidly, currently enabling higher throughputs at lower costs. Yet as multi-omics moves from research to routine care, the central challenge is no longer data generation, but standardizing and interpreting complexity within health systems built for discrete tests. In this Perspective, we chart the path from assay to implementation by demonstrating how integrative analyses outperform single modalities, as well as by emphasizing that multiplexing, high dimensionality and probabilistic interpretation introduce risks to reproducibility and clinical validity. We examine computational strategies for multimodal integration, highlighting the importance of explainable AI for auditability and regulatory trust. Drawing on lessons from early national programs, we suggest that scalable clinical adoption depends on interoperable digital infrastructures, harmonized quality standards and multidisciplinary care models that embed multi-omics into everyday practice.
| Original language | English |
|---|---|
| Number of pages | 14 |
| Journal | Nature Genetics |
| Early online date | Jul 2026 |
| DOIs | |
| Publication status | E-pub ahead of print - Jul 2026 |
Keywords
- Central-nervous-system
- Classification
- Cost-effectiveness
- Health
- Identify
- Integration
- Molecular-pathology
- Proteomics
- Standards
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