PreprintCited by 28Single-cell and spatial transcriptomicsBioinformatics and Genomic NetworksGene Regulatory Network Analysis

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scMODAL: A general deep learning framework for comprehensive single-cell multi-omics data alignment with feature links

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Preprint — published as 10.1038/s41467-025-60333-z · Paper page

Abstract

Recent advancements in single-cell technologies have enabled comprehensive characterization of cellular states through transcriptomic, epigenomic, and proteomic profiling at single-cell resolution. These technologies have significantly deepened our understanding of cell functions and disease mechanisms from various omics perspectives. As these technologies evolve rapidly and data resources expand, there is a growing need for computational methods that can integrate information from different modalities to facilitate joint analysis of single-cell multi-omics data. However, integrating single-cell omics datasets presents unique challenges due to varied feature correlations and technology-specific limitations. To address these challenges, we introduce scMODAL, a deep learning framework tailored for single-cell multi-omics data alignment using feature links. scMODAL integrates datasets with limited known positively correlated features, leveraging neural networks and generative adversarial networks to align cell embeddings and preserve feature topology. Our experiments demonstrate scMODAL’s effectiveness in removing unwanted variation, preserving biological information, and accurately identifying cell subpopulations across diverse datasets. scMODAL not only advances integration tasks but also supports downstream analyses such as feature imputation and feature relationship inference, offering a robust solution for advancing single-cell multi-omics research.

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Metadata

Authors
Wang, G., Zhao, J., Lin, Y., Liu, T., Zhao, Y., & Zhao, H.
Affiliations
Yale University (US)
Corresponding author
Zhao, Hongyu
Venue
Nature Communications
Publisher
openRxiv
Published
2024-10-03
Volume
16
Issue
1
Pages
4994-4994
ISSN
2041-1723 (ISSN-L)
OpenAlex
W4410855348
Cited by
28
References
1
Citations by year
2026: 20 · 2025: 8
FWCI
8.30
Type
journal article
Language
en
Open access
Locations
  • Nature Communications (publishedVersion, cc-by-nc-nd)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • U.S. Department of Health and Human Services (RF1 AG081413, R01 AG068191, R01 EB034720, P50CA196530, R01 GM134005, U24 HG012108)
  • National Institutes of Health (1rf1ag081413-01, CA196530)
  • National Institute on Aging (RF1AG068191, RF1 AG081413, R01AG068191)
  • National Human Genome Research Institute (U24HG012108)
  • National Cancer Institute (P50CA196530)
  • National Institute of General Medical Sciences (R01GM134005)
  • National Institute of Biomedical Imaging and Bioengineering (R01EB034720)
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 › Gene Regulatory Network Analysis
Keywords
single-cell multi-omics integration, cell embedding, generative adversarial networks, feature imputation, cell subpopulation identification, transcriptomics, epigenomics, proteomics
MeSH terms
Deep Learning, Multiomics, Humans, Neural Networks, Computer, Computational Biology, Gene Expression Profiling, Genomics, Proteomics, Epigenomics, Single-Cell Analysis, Transcriptome

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