Comprehensively characterizing cellular diversity is critical for understanding tissue development, identifying disease-associated populations and investigating gene programmes linked to specialized functions. Advances in single-cell profiling reveal additional cell-specific transcripts and molecular associations, yet many foundation models represent only a restricted portion of this increasingly rich molecular information. Here we present CellNet, which enables panoramic modelling of single-cell transcriptomes by integrating DNA-derived gene identities and measured RNA expression in a shared image representation. Pretrained on 231 million cell profiles spanning 40 species, CellNet improves rare-population and condition-associated state recognition in evaluated cohorts while retaining competitive general cell representations. It predicts withheld coding-gene expression and selected non-coding targets in total-RNA data, and recovers lineage-specific expression patterns in spatial measurements. Prediction also extends across species, including to targets without expression-pretraining exposure. Its gene representations retrieve known non-coding modules and developmental or neural programmes, including from sparsely detected RNA queries. Together, these results establish CellNet as a scalable framework for interpreting cellular diversity through increasingly comprehensive transcriptomic measurements.
This study introduces CellART, a unified framework designed to extract single-cell information across diverse high-resolution spatial transcriptomics platforms, including VisiumHD, Xenium, MERFISH, and Stereo-seq, and highlights its ability to fully leverage high-resolution ST data.
Yu-Heng Chen, Yu-Yao Liu, Zhi-Wei Wang et al.· bioRxiv· 1 citation
Single-cell transcriptomics enables profiling of cellular states at unprecedented resolution, but its high dimensionality, sparsity, and technical batch effects pose significant challenges for representation learning. Existing single-cell foundation models typically encode each cell independently or only model cells fr...
Su-Yuan Zhao, Ming-Hao Liu, Yi-Zhen Luo et al.· 0 citations
It is demonstrated that scTransMIL accurately predicts sample-level cancer phenotypes, including the tissue-of-origin for metastatic tumors, and robustly identifies tumor-associated cell populations and maps biological progression trajectories using only minimal sample-level annotations.
Zhen-Chao Tang, Fang Wang, Fan Yang et al.· Nature Communications· 2 citations
Single-cell proteomics provides a direct functional readout of cellular states, but targeted assays measure limited and non-identical protein panels, fragmenting information across experiments. Here, we present ProtCell, a foundation model developed using approximately 380 million cells from 98 datasets for pretraining...
Single-cell technologies enable epigenomics characterization at single-cell resolution, offering novel insights into gene expression regulation and a wide range of biological processes, including cell fate determination, developmental differentiation, and environmental adaptation. In recent years, plant single-cell epi...
Cheng Tong, Chao-Fan Liu, Zhe Liang et al.· The Plant Cell· 0 citations
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