bioRxivBioinformaticsPreprint
CellPLM: Pre-training of Cell Language Model Beyond Single Cells
Hongzhi WeniD, Wenzhuo TangiD, Xinnan Dai, Jiayuan DingiD, Wei JiniD, Yuying XieiD, Jiliang TangiD
Abstract
The current state-of-the-art single-cell pre-trained models are greatly inspired by the success of large language models. They trained transformers by treating genes as tokens and cells as sentences. However, three fundamental differences between single-cell data and natural language data are overlooked: (1) scRNA-seq data are presented as bag-of-genes instead of sequences of RNAs; (2) Cell-cell relations are more intricate and important than inter-sentence relations; and (3) The quantity of single-cell data is considerably inferior to text data, and they are very noisy. In light of these characteristics, we propose a new pre-trained model CellPLM, which takes cells as tokens and tissues as sentences. In addition, we leverage spatially-resolved transcriptomic data in pre-training to facilitate learning cell-cell relationships and introduce a Gaussian mixture prior distribution as an additional inductive bias to overcome data limitation. CellPLM is the first single-cell pre-trained transformer that encodes cell-cell relations and it consistently outperforms existing pre-trained and non-pre-trained models in diverse downstream tasks, with 100x times higher inference speed compared to existing pre-trained models.
Abstract summary
Claude Opus 5.5 · xhigh effort · 18 Oct 2026 · from the abstract · CC BY-NC-ND 4.0
Treating cells as tokens and tissues as sentences, with spatial transcriptomics added during pre-training, gives a single-cell foundation model the authors report outperforms existing models and runs far faster.
Single-cell pre-trained models have borrowed the language-model recipe of genes as tokens and cells as sentences, which ignores that expression profiles are unordered, that cells relate to their neighbours, and that single-cell corpora are small and noisy next to text. CellPLM changes the unit of modelling to the cell inside a tissue and uses spatial data plus a distributional prior to compensate for the limited training corpus.
Key results
ClaimedCellPLM pre-trains over cells as tokens and tissues as sentences, which the authors present as the first single-cell pre-trained transformer to encode relations between cells rather than only within one cell.
Priority claim stated in the abstract; no architecture details, corpus size or ablation separating the cell-as-token design from the rest is given. · Abstract
ClaimedSpatially resolved transcriptomics is used during pre-training to supply cell-cell relationships, and a Gaussian mixture prior is imposed as an inductive bias against the small, noisy training corpus.
Both design choices are described in the abstract without an ablation quantifying what either contributes. · Abstract
ClaimedAcross downstream tasks the model is reported to beat both pre-trained and non-pre-trained competitors while running much faster at inference.
A 100x inference speedup over existing pre-trained models is claimed; the abstract names no task, dataset, metric or competing model, and gives no accuracy numbers. · Abstract
Methods, data and reproducibility
A transformer pre-trained with cells as tokens and tissues as sentences, drawing on single-cell and spatially resolved transcriptomic data so that cell-cell relations enter the representation, with a Gaussian mixture prior as an extra inductive bias; evaluated on unnamed downstream tasks against pre-trained and non-pre-trained baselines.
- scRNA-seq profiles used for pre-training
- Spatially resolved transcriptomic data used during pre-training to supply cell-cell relations
- Methods & tools
- CellPLM
- Reproducibility gaps
- No repository, model weights, dataset identifiers or hardware details appear; the inference-speed claim has no stated measurement setting.
Limitations (3)
- The authors note that single-cell data are far scarcer and noisier than text corpora, which is why an explicit prior is added rather than relying on scale. · stated by the authors
- No downstream task, dataset, metric or baseline is named, so neither the accuracy gain nor the speedup can be checked or placed against specific competitors. · noted in this summary
- Pre-training depends on spatially resolved transcriptomics, and the abstract does not say which platforms or tissues that covers or how well the model transfers beyond them. · noted in this summary
Read this if you work with single-cell foundation models and care whether modelling cells in tissue context beats gene-token designs, or need fast inference.
- Citations
- 76
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