ArticleBioinformatics (Oxford, England)2026
Cell-o1 : training LLMs to solve single-cell reasoning puzzles with reinforcement learning.
Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
4 citing papers in PubMed.
- CellDuality: Unlocking Biological Reasoning in LLMs with Self-Supervised RLVR.... International Conference on Learning Representations · 2026Article
- TissueNarrator: Generative Modeling of Spatial Transcriptomics with Large Language Models.bioRxiv : the preprint server for biology · 2025Article
- Article
- ProtLoc-GRPO: Cell line-specific subcellular localization prediction using a graph-based model and reinforcement learning.bioRxiv : the preprint server for biology · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
motivationLarge language models (LLMs) have demonstrated strong general reasoning abilities, but applying them to domain-specific tasks such as analysing single-cell RNA sequencing data remains a challenge. A central task in this domain is cell type annotation, which is critical for understanding cellular heterogeneity. Although recent foundation models attempt to automate this process, they typically annotate cells independently, without considering batch-level context or providing explanatory reasoning. To address this limitation, we introduce the CellPuzzles benchmark, which reformulates cell type annotation as a batch-level reasoning task. CellPuzzles spans diverse tissues, diseases, and donor conditions, and requires reasoning across the batch-level cellular context to ensure label uniqueness.
resultsWe find that off-the-shelf LLMs struggle on this task, with the best baseline (OpenAI o1) achieving only 19.0% batch-level accuracy. To fill this gap, we propose Cell-o1, a 7B LLM trained via supervised fine-tuning on distilled reasoning traces, followed by reinforcement learning with batch-level rewards. Cell-o1 achieves state-of-the-art performance, outperforming OpenAI o1 by over 73% and generalizing well across contexts. Further analysis of training dynamics and reasoning behaviors provides insights into batch-level annotation performance and emergent expert-like reasoning. AVAILABILITY AND IMPLEMENTATION: Code and data are available at https://github.com/ncbi-nlp/cell-o1.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.