Skip to content
aiqbench takeMachine Learning

aiqbench analysis

This research introduces a novel two-stage framework combining flow matching and reinforcement learning to model the evolutionary dynamics of RNA sequence variation, addressing limitations in existing inverse-folding methods. By coupling coordinated sequence variation with thermodynamic selection, the approach achieves state-of-the-art performance on standard benchmarks while offering new insights into policy dynamics and robustness.
Source coveringarXiv
What this isA model's reading of the article and related coverage, written for aiqbench. Not the publisher's words.

RNA Design via Conditioned Flow Matching and Finite-Policy Reinforcement Learning

arXiv2 min read

arXiv:2609.36885v1 Announce Type: cross Abstract: RNA design aims to identify sequences that fold into specified secondary structures. Existing methods formulate the task as target-specific search or conditional generation. However, natural RNA evolution proceeds through sequence variation and selection, with compensatory substitutions, whereas these methods do not explicitly model this process. To address this limitation, we propose a two-stage framework comprising RNA Inverse-Folding Flow (RNA-IFlow) and RNA-IFlow-RL. RNA-IFlow uses structure-conditioned Dirichlet Flow Matching to model coordinated variation across the sequence, while RNA-IFlow-RL maps the learned flow to a pairing-preserving finite policy and refines it with thermodynamic feedback. Our framework achieves leading performance on multiple benchmarks, reaching 85.19% Pass@1 on Rfam-27. Further analyses reveal thermodynamic gains, policy dynamics, and robustness across settings. Our work couples coordinated variation with thermodynamic selection, offering a novel paradigm for RNA design.

Abstract:RNA design aims to identify sequences that fold into specified secondary structures. Existing methods formulate the task as target-specific search or conditional generation. However, natural RNA evolution proceeds through sequence variation and selection, with compensatory substitutions, whereas these methods do not explicitly model this process. To address this limitation, we propose a two-stage framework comprising RNA Inverse-Folding Flow (RNA-IFlow) and RNA-IFlow-RL. RNA-IFlow uses structure-conditioned Dirichlet Flow Matching to model coordinated variation across the sequence, while RNA-IFlow-RL maps the learned flow to a pairing-preserving finite policy and refines it with thermodynamic feedback. Our framework achieves leading performance on multiple benchmarks, reaching 85.19% Pass@1 on Rfam-27. Further analyses reveal thermodynamic gains, policy dynamics, and robustness across settings. Our work couples coordinated variation with thermodynamic selection, offering a novel paradigm for RNA design.

32 pages, figures. Preprint

Biomolecules (q-bio.BM); Machine Learning (cs.LG)

arXiv:2609.36885 [q-bio.BM]

(or arXiv:2609.36885v1 [q-bio.BM] for this version)

https://doi.org/10.48550/arXiv.2609.36885 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

arXivLabs is a framework that allows collaborators to develop and share new arXiv features directly on our website.

Both individuals and organizations that work with arXivLabs have embraced and accepted our values of openness, community, excellence, and user data privacy. arXiv is committed to these values and only works with partners that adhere to them.

Have an idea for a project that will add value for arXiv's community? Learn more about arXivLabs.

Full text under the publisher's open licence · 230 words

Related coverage