CMOT: cross-modality optimal transport for multimodal inference
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Abstract
Multimodal measurements of single-cell sequencing technologies facilitate a comprehensive understanding of specific cellular and molecular mechanisms. However, simultaneous profiling of multiple modalities of single cells is challenging, and data integration remains elusive due to missing modalities and cell-cell correspondences. To address this, we developed a computational approach, Cross-Modality Optimal Transport (CMOT), which aligns cells within available multi-modal data (source) onto a common latent space and infers missing modalities for cells from another modality (target) of mapped source cells. CMOT outperforms existing methods in various applications from developing brain, cancers to immunology, and provides biological interpretations improving cell-type or cancer classifications.
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A contrastive loss brings related modality pairs closer and distances unrelated pairs in a shared embedding space.
“The model is trained using a contrastive loss function to bring related modality pairs, like images and descriptions, closer in a shared embedding space while distancing unrelated pairs [179,180].”
From Multimodal fusion and vision–language models: A survey for robot vision (2026) · cites this paper as [179]
The Methods section (page unavailable) says CMOT projects modalities into a common manifold and minimizes distances between corresponding samples. It describes manifold alignment and optimal transport, not a contrastive loss that distances unrelated pairs; its examples concern single-cell modalities, not images and descriptions. (LLM, conf=0.88)
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“…model employs specialized encoders (e.g., convolutional neural networks for visual data, transformer architectures for text and audio data) [178, 179] to extract features from different modalities, and then interacts and integrates these features through cross-modal alignment mechanisms [180, 181].”
- Authors
- Alatkar, S. A., & Wang, D.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Wang, Daifeng
- Venue
- Genome biology
- Published
- 2023-07-11
- Volume
- 24
- Issue
- 1
- Pages
- 163-163
- ISSN
- 1465-6906 (ISSN-L)
- 1474-760X
- PMC
- PMC10334579
- OpenAlex
- W4383878671
- Cited by
- 24
- References
- 44
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 8 · 2023: 3
- FWCI
- 2.14
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Genome biology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Science Foundation (2144475)
- University of Wisconsin-Madison
- Waisman Center (P50HD105353)
- National Institutes of Health (1r21ns128761-01)
- National Institute on Aging (R01AG067025)
- National Institute of Mental Health (U01MH116492)
- National Cancer Institute (R21CA237955)
- National Institute of Neurological Disorders and Stroke (R21NS128761, R03NS123969, R21NS127432)
- Division of Graduate Education
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (P50HD105353)
- 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
- multimodal single-cell data, cell alignment, latent space embedding, data integration, cell type classification, cancer classification
- MeSH terms
- Single-Cell Analysis
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