Methods and applications for single-cell and spatial multi-omics
Open accessAbstract
The joint analysis of the genome, epigenome, transcriptome, proteome and/or metabolome from single cells is transforming our understanding of cell biology in health and disease. In less than a decade, the field has seen tremendous technological revolutions that enable crucial new insights into the interplay between intracellular and intercellular molecular mechanisms that govern development, physiology and pathogenesis. In this Review, we highlight advances in the fast-developing field of single-cell and spatial multi-omics technologies (also known as multimodal omics approaches), and the computational strategies needed to integrate information across these molecular layers. We demonstrate their impact on fundamental cell biology and translational research, discuss current challenges and provide an outlook to the future.
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Rapid development of spatial transcriptomics has provided information on local tissue contexts and adjacent cellular interactions.
“The rapid development of spatial transcriptomics has provided information on local tissue contexts and adjacent cellular interactions [122,123].”
From Challenges in AI-driven Biomedical Multimodal Data Fusion and Analysis (2025) · cites this paper as [122]
Single-cell multiomics approaches, by jointly measuring multiple molecular types, empowered the dissection of crosstalk across distinct molecular modalities.
“Single-cell multiomics approaches, by jointly measuring multiple molecular types, empowered the dissection of the crosstalk across distinct molecular modalities32.”
From Single-cell parallel analysis of DNA damage and transcriptome reveals selective genome vulnerability (2025) · cites this paper as [32]
Senescence classifiers can detect senescence in vivo in aging, fibrosis, preclinical cancer models, and clinical samples.
“These new senescence classifiers can detect senescence in vivo in aging, fibrosis, preclinical models of cancer140,141, and a range of clinical samples141,142.”
From Guidelines for minimal information on cellular senescence experimentation in vivo (2024) · cites this paper as [141]
The Single-cell genomics-plus-transcriptomics section discusses cancer cell states and how multi-omics methods may help study ageing, but it does not discuss senescence classifiers. Searches for senescence classifiers, fibrosis, and detection in clinical samples found no passage supporting the attributed claim. (LLM, conf=0.75)
Experimental — accuracy not yet measuredMultiparameter morphological analysis is a robust, unbiased, and quantifiable marker of senescence.
“Advances in high-throughput imaging, computational tools, and machine learning have fostered the use of multiparameter morphological analysis as a robust, unbiased, and quantifiable marker of senescence.”
From Guidelines for minimal information on cellular senescence experimentation in vivo (2024) · cites this paper as [141]
The Data integration section discusses combining cell morphology images with expression data to identify cellular subpopulations, and the Perspectives section mentions studying ageing. Neither says that multiparameter morphological analysis is a robust, unbiased, quantifiable marker of senescence. Searches for senescence, high-throughput imaging, and morphological markers found no passage making that claim. (LLM, conf=0.76)
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- Authors
- Vandereyken, K., Sifrim, A., Thienpont, B., & Voet, T.
- Affiliations
- Aligning Science Across Parkinson's (US)
- Corresponding author
- Voet, Thierry
- Venue
- Nature Reviews Genetics
- Published
- 2023-03-02
- Volume
- 24
- Issue
- 8
- Pages
- 494-515
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- PMC
- PMC9979144
- OpenAlex
- W4322768301
- Cited by
- 1,244
- References
- 189
- Citations by year
- 2026: 355 · 2025: 408 · 2024: 337 · 2023: 141 · 2022: 2 · 2013: 1
- FWCI
- 32.65
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Lirias (submittedVersion, other-oa)
- Funders
- Michael J. Fox Foundation for Parkinson's Research (ASAP-000430)
- Leona M. and Harry B. Helmsley Charitable Trust (1903-03785)
- Fonds Wetenschappelijk Onderzoek (G081318N, G088621N, G0C7519N, S003422N, G0C6120N, I001818N)
- KU Leuven (C14/18/092, C24M/19/075, C14/22/125, METH/21/06, IDN/21/006, IDN/19/039)
- Vlaamse regering (S003422N)
- Fondation contre le Cancer
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- single-cell multi-omics, spatial multi-omics, single-cell genomics, single-cell transcriptomics, single-cell epigenomics, single-cell proteomics, single-cell metabolomics, translational research
- MeSH terms
- Multiomics, Genome, Proteome, Metabolome, Single-Cell Analysis, Transcriptome
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