Designing RNAs with Language Models

Fuente: arXiv
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Main Authors: Gautam, Milan, Dai, Ning, Zhou, Tianshuo, Xie, Bowen, Mathews, David, Huang, Liang
Format: Preprint
Published: 2026
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author Gautam, Milan
Dai, Ning
Zhou, Tianshuo
Xie, Bowen
Mathews, David
Huang, Liang
author_facet Gautam, Milan
Dai, Ning
Zhou, Tianshuo
Xie, Bowen
Mathews, David
Huang, Liang
contents RNA design, the task of finding a sequence that folds into a target secondary structure, has broad biological and biomedical impact but remains computationally challenging due to the exponentially large sequence space and exponentially many competing folds. Traditional approaches treat it as an optimization problem, relying on per-instance heuristics or constraint-based search. We instead reframe RNA design as conditional sequence generation and introduce a reusable neural approximator, instantiated as an autoregressive language model (LM), that maps target structures directly to sequences. We first train our model in a supervised setting on random-induced structure-sequence pairs, and then use reinforcement learning (RL) to optimize end-to-end metrics. We also propose methods to select a small subset for RL that greatly improves RL efficiency and quality. Across four datasets, our approach outperforms state-of-the-art systems on key metrics such as Boltzmann probability while being 1.7x faster, establishing conditional LM generation as a scalable, task-agnostic alternative to per-instance optimization for RNA design. Our code and data are available at https://github.com/KuNyaa/RNA-Design-LM.
format Preprint
id arxiv_https___arxiv_org_abs_2602_12470
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Designing RNAs with Language Models
Gautam, Milan
Dai, Ning
Zhou, Tianshuo
Xie, Bowen
Mathews, David
Huang, Liang
Machine Learning
Artificial Intelligence
RNA design, the task of finding a sequence that folds into a target secondary structure, has broad biological and biomedical impact but remains computationally challenging due to the exponentially large sequence space and exponentially many competing folds. Traditional approaches treat it as an optimization problem, relying on per-instance heuristics or constraint-based search. We instead reframe RNA design as conditional sequence generation and introduce a reusable neural approximator, instantiated as an autoregressive language model (LM), that maps target structures directly to sequences. We first train our model in a supervised setting on random-induced structure-sequence pairs, and then use reinforcement learning (RL) to optimize end-to-end metrics. We also propose methods to select a small subset for RL that greatly improves RL efficiency and quality. Across four datasets, our approach outperforms state-of-the-art systems on key metrics such as Boltzmann probability while being 1.7x faster, establishing conditional LM generation as a scalable, task-agnostic alternative to per-instance optimization for RNA design. Our code and data are available at https://github.com/KuNyaa/RNA-Design-LM.
title Designing RNAs with Language Models
topic Machine Learning
Artificial Intelligence
url https://arxiv.org/abs/2602.12470