henhaobio
Sign in

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

PDFDOI

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

  1. 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

  2. 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

  3. 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

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISWaele '26Li '24Xiao '25Bahrami '25Fang '25Rizvi '25
79% semantic matchBioinformatics
Gaetan De Waele, Gerben Menschaert, Willem Waegeman·NAR Genomics and Bioinformatics·Jun 27, 2026· 2 citations