Evidence map›Paper›PMID 41714588›Full record

ArticleNature communications2026

SamplingDesign: RNA design via continuous optimization with coupled variables and Monte-Carlo sampling.

Wei Yu Tang, Ning Dai, Tianshuo Zhou, David H Mathews, Liang Huang

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Wei Yu TangSchool of EECS, Oregon State University, Corvallis, OR, USA.ORCID http://orcid.org/0009-0008-1141-9479
Ning DaiSchool of EECS, Oregon State University, Corvallis, OR, USA.
Tianshuo ZhouSchool of EECS, Oregon State University, Corvallis, OR, USA.ORCID http://orcid.org/0009-0008-4804-0825
David H MathewsDept. of Biochemistry & Biophysics, University of Rochester Medical Center, Rochester, NY, USA.ORCID http://orcid.org/0000-0002-2907-6557
Liang HuangSchool of EECS, Oregon State University, Corvallis, OR, USA. liang.huang.sh@gmail.com.ORCID http://orcid.org/0000-0001-6444-7045

Funding

National Science Foundation (NSF) 2009071National Science Foundation (NSF) 2330737
6 · The paper itself

Abstract

RNA design aims to find a sequence that can fold into a target secondary structure. It can create artificial RNA molecules for specific functions, with wide applications in medicine. It is computationally challenging due to two levels of combinatorial explosion: the exponentially large design space and the exponentially many competing structures per design. Popular methods such as local search cannot keep up with these combinatorial explosions. We instead employ two techniques from machine learning, continuous optimization and Monte-Carlo sampling. We start from a distribution over all valid sequences, and use gradient descent to improve the expectation of an arbitrary objective function. We define novel coupled-variable distributions to model the correlation between nucleotides. We then use sampling to approximate the objective, estimate the gradient, and select the final candidate. Our work consistently outperforms state-of-the-art methods in key metrics including Boltzmann probability and ensemble defect, especially on long and hard-to-design structures.

Indexed as

RNAAlgorithmsMachine LearningMonte Carlo MethodNucleic Acid ConformationRNA

Identifiers

PMID41714588
PMCPMC13031908

What OpenQuestion holds

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Registered trials

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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.