Evidence map›Paper›PMID 36192461›Full record

ArticleNature methods2022

RNA secondary structure packages evaluated and improved by high-throughput experiments.

Hannah K Wayment-Steele, Wipapat Kladwang, Alexandra I Strom, Jeehyung Lee, Adrien Treuille, Alex Becka, Eterna Participants, Rhiju Das

Open access · bronzeAbstract read
In one paragraph

Article in Nature methods, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
10.4field-weighted citation impact, top 1% of its field
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

80 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Maintaining transcriptome solubility constrains mRNA sequence composition.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  3. Markov models of SHAPE data improve secondary structure prediction.bioRxiv : the preprint server for biology · 2026
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  4. A passive protein environment offsets RNA folding energetics in cells.bioRxiv : the preprint server for biology · 2026
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  5. Article
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  7. Machine Learning for RNA-Targeting Drug Design.Journal of chemical information and modeling · 2026
    Review
  8. De novo design of RNA pseudoknots with deep learning.bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. bioRxiv : the preprint server for biology · 2026
    Article
  16. Article
  17. RNA Structure and Its Function.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  18. Article
  19. Article
  20. Article

20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Hannah K Wayment-SteeleDepartment of Chemistry, Stanford University, Stanford, CA, USA.
Wipapat KladwangEterna Massive Open Laboratory, Stanford, CA, USA.
Alexandra I StromDepartment of Biochemistry, Stanford University, Stanford, CA, USA.
Jeehyung LeeEterna Massive Open Laboratory, Stanford, CA, USA.
Adrien TreuilleEterna Massive Open Laboratory, Stanford, CA, USA.
Alex BeckaDepartment of Biochemistry, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-1552-4881
Eterna Participants
Rhiju DasEterna Massive Open Laboratory, Stanford, CA, USA. rhiju@stanford.edu.ORCID http://orcid.org/0000-0001-7497-0972
Eterna Massive Open Laboratory · USStanford University · USSan Diego State University · US

Funding

Next-generation computational/chemical methods for complex RNA structuresR35GM122579 · NIGMS · STANFORD UNIVERSITY · PI Rhiju Das · 2017 to 2026
$7.2M
NIGMS NIH HHS R35 GM122579
6 · The paper itself

Abstract

Despite the popularity of computer-aided study and design of RNA molecules, little is known about the accuracy of commonly used structure modeling packages in tasks sensitive to ensemble properties of RNA. Here, we demonstrate that the EternaBench dataset, a set of more than 20,000 synthetic RNA constructs designed on the RNA design platform Eterna, provides incisive discriminative power in evaluating current packages in ensemble-oriented structure prediction tasks. We find that CONTRAfold and RNAsoft, packages with parameters derived through statistical learning, achieve consistently higher accuracy than more widely used packages in their standard settings, which derive parameters primarily from thermodynamic experiments. We hypothesized that training a multitask model with the varied data types in EternaBench might improve inference on ensemble-based prediction tasks. Indeed, the resulting model, named EternaFold, demonstrated improved performance that generalizes to diverse external datasets including complete messenger RNAs, viral genomes probed in human cells and synthetic designs modeling mRNA vaccines.

Indexed as

AlgorithmsRNAHumansNucleic Acid ConformationProtein Structure, SecondaryThermodynamicsRNA

Identifiers

PMID36192461
PMCPMC9839360
OpenAlexW4300861274

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.