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scMomer reveals robust multi-omics representations in single-cell data, indicating enhanced cellular insights despite missing modalities.
Foundation models offer new opportunities to capture cellular behavior from large-scale single-cell data. However, their development has been greatly constrained due to the limited availability of multi-omics profiles. Consequently, most models are designed for a single modality (e.g. scRNA-seq, or scATAC-seq, etc.), restricting their ability to capture the diversity of heterogeneous biological systems. Here, we introduce scMomer, a modality-aware pretraining framework designed for multi-modal representation learning under missing modality conditions. scMomer adopts a three-stage pretraining strategy that learns unimodal cell representations, models joint representations from multi-omics data, and distills multi-modal knowledge to enable multi-omics-like representations from unimodal input. Its modality-specific architecture and three-stage pretraining strategy enable effective learning under missing modality conditions and help capture cellular heterogeneity. Through extensive experiments, scMomer generates biologically meaningful embeddings and outperforms state-of-the-art unimodal approaches across diverse gene-level and cell-level downstream tasks, including cross-modality translation, gene function prediction, cell annotation, drug response prediction, and perturbation prediction. Overall, these results demonstrate that scMomer serves as a robust, generalizable, and scalable foundation for single-cell multi-modal analysis under missing modality conditions.
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Liu et al. (2025) studied this question.
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