Evidence map›Paper›PMID 42559559›Full record

Article... International Conference on Learning Representations2026

CellDuality: Unlocking Biological Reasoning in LLMs with Self-Supervised RLVR.

Yuhang Chen, Zhen Tan, Ruichen Zhang, Mufan Qiu, Tianlong Chen

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Article in ... International Conference on Learning Representations, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Yuhang ChenUniversity of North Carolina at Chapel Hill.
Zhen TanArizona State University.
Ruichen ZhangUniversity of North Carolina at Chapel Hill.
Mufan QiuUniversity of North Carolina at Chapel Hill.
Tianlong ChenUniversity of North Carolina at Chapel Hill.

Funding

Robust and Interpretable Multi-modal AI/ML for Precision MedicineR01EB037101 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Tianlong Chen · 2025 to 2026
$1.4M
NIBIB NIH HHS R01 EB037101
6 · The paper itself

Abstract

Developing generalist large language models (LLMs) capable of complex biological reasoning is a central challenge in computational biology. While existing LLMs excel at predictive tasks like cell type annotation and logically-constrained problems, enabling open-ended and mechanistic reasoning remains a challenge. A promising direction is Reinforcement Learning from Verifiable Rewards (RLVR), which has been shown to significantly enhance complex reasoning in general domains like mathematics and code synthesis. However, its application in biology is hindered, as most biological outcomes are non-verifiable. For example, verifying a generated gene sequence is usually infeasible. In this paper, we introduce CellDuality, a self-supervised framework that enables LLM agents for robust reasoning in single-cell biology. Our framework is built on the principle of complementary task duality, a self-verification process that leverages a bidirectional reasoning loop. First, the model performs a forward reasoning task by predicting a biological outcome (e.g., a cell's response to a drug). Then, in a complementary inverse task, it must reason backward from its own prediction to reconstruct the initial conditions (e.g., the original drug perturbation). The fidelity of this reconstruction serves as an intrinsic reward signal, creating a feedback loop that enforces logical and biological consistency. We use these intrinsic rewards to align the base LLM via reinforcement learning, without requiring ground-truth verification labels. We demonstrate that CellDuality achieves state-of-the-art performance and provides coherent biological explanations across a diverse suite of single-cell reasoning tasks. Critically, on the challenging out-of-distribution perturbation prediction benchmark, our self-supervised approach significantly outperforms the standard fine-tuning baseline and narrows the performance gap to a supervised RLVR baseline. Our work showcases a new path toward scalable training of biological foundation models.

Identifiers

PMID42559559
PMCPMC13441433

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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.