Evidence map›Paper›PMID 39811444›Full record

ArticleBiology methods & protocols2025

Robust RNA secondary structure prediction with a mixture of deep learning and physics-based experts.

Xiangyun Qiu

Abstract read
In one paragraph

Article in Biology methods & protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

1 author.

Xiangyun QiuDepartment of Physics, George Washington University, Washington, DC 20052, United States.ORCID https://orcid.org/0000-0002-2600-5032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A mixture-of-experts (MoE) approach has been developed to mitigate the poor out-of-distribution (OOD) generalization of deep learning (DL) models for single-sequence-based prediction of RNA secondary structure. The main idea behind this approach is to use DL models for in-distribution (ID) test sequences to leverage their superior ID performances, while relying on physics-based models for OOD sequences to ensure robust predictions. One key ingredient of the pipeline, named MoEFold2D, is automated ID/OOD detection via consensus analysis of an ensemble of DL model predictions without requiring access to training data during inference. Specifically, motivated by the clustered distribution of known RNA structures, a collection of distinct DL models is trained by iteratively leaving one cluster out. Each DL model hence serves as an expert on all but one cluster in the training data. Consequently, for an ID sequence, all but one DL model makes accurate predictions consistent with one another, while an OOD sequence yields highly inconsistent predictions among all DL models. Through consensus analysis of DL predictions, test sequences are categorized as ID or OOD. ID sequences are subsequently predicted by averaging the DL models in consensus, and OOD sequences are predicted using physics-based models. Instead of remediating generalization gaps with alternative approaches such as transfer learning and sequence alignment, MoEFold2D circumvents unpredictable ID-OOD gaps and combines the strengths of DL and physics-based models to achieve accurate ID and robust OOD predictions.

Indexed as

deep learningmigrant workersmixture of expertsphysics-based algorithmsRNA structure

Identifiers

PMID39811444
PMCPMC11729747

What OpenQuestion holds

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Read underepoch 390

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.