Evidence map›Paper›PMID 39775709›Full record

ArticleBioinformatics (Oxford, England)2024

RNA-TorsionBERT: leveraging language models for RNA 3D torsion angles prediction.

Clément Bernard, Guillaume Postic, Sahar Ghannay, Fariza Tahi

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

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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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

4 authors.

Clément BernardUniversité Paris Saclay, Univ Evry, IBISC, Evry-Courcouronnes 91020, France.ORCID 0009-0003-0117-9823
Guillaume PosticUniversité Paris Saclay, Univ Evry, IBISC, Evry-Courcouronnes 91020, France.ORCID 0000-0002-0380-0092
Sahar GhannayLISN-CNRS/Université Paris-Saclay, Orsay 91400, France.ORCID 0000-0002-7531-2522
Fariza TahiUniversité Paris Saclay, Univ Evry, IBISC, Evry-Courcouronnes 91020, France.ORCID 0000-0002-3975-5668

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationPredicting the 3D structure of RNA is an ongoing challenge that has yet to be completely addressed despite continuous advancements. RNA 3D structures rely on distances between residues and base interactions but also backbone torsional angles. Knowing the torsional angles for each residue could help reconstruct its global folding, which is what we tackle in this work. This paper presents a novel approach for directly predicting RNA torsional angles from raw sequence data. Our method draws inspiration from the successful application of language models in various domains and adapts them to RNA.

resultsWe have developed a language-based model, RNA-TorsionBERT, incorporating better sequential interactions for predicting RNA torsional and pseudo-torsional angles from the sequence only. Through extensive benchmarking, we demonstrate that our method improves the prediction of torsional angles compared to state-of-the-art methods. In addition, by using our predictive model, we have inferred a torsion angle-dependent scoring function, called TB-MCQ, that replaces the true reference angles by our model prediction. We show that it accurately evaluates the quality of near-native predicted structures, in terms of RNA backbone torsion angle values. Our work demonstrates promising results, suggesting the potential utility of language models in advancing RNA 3D structure prediction. AVAILABILITY AND IMPLEMENTATION: Source code is freely available on the EvryRNA platform: https://evryrna.ibisc.univ-evry.fr/evryrna/RNA-TorsionBERT.

Indexed as

Computational BiologyNucleic Acid ConformationRNAAlgorithmsModels, MolecularRNA

Identifiers

PMID39775709
PMCPMC11758789

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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.