Evidence map›Paper›PMID 31776342›Full record

ArticleNature communications2019

RNA secondary structure prediction using an ensemble of two-dimensional deep neural networks and transfer learning.

Jaswinder Singh, Jack Hanson, Kuldip Paliwal, Yaoqi Zhou

Abstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 183 papers.

0numbers the graph read from it
0cells of the map it votes in
183citing 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

183 citing papers in PubMed.

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  14. Large language models for bioinformatics.Quantitative biology (Beijing, China) · 2026
    Review
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123 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

4 authors.

Jaswinder SinghSignal Processing Laboratory, School of Engineering and Built Environment, Griffith University, Brisbane, QLD, 4111, Australia.ORCID http://orcid.org/0000-0002-0478-5533
Jack HansonSignal Processing Laboratory, School of Engineering and Built Environment, Griffith University, Brisbane, QLD, 4111, Australia.ORCID http://orcid.org/0000-0001-6956-6748
Kuldip PaliwalSignal Processing Laboratory, School of Engineering and Built Environment, Griffith University, Brisbane, QLD, 4111, Australia. k.paliwal@griffith.edu.au.ORCID http://orcid.org/0000-0002-3553-3662
Yaoqi ZhouInstitute for Glycomics and School of Information and Communication Technology, Griffith University, Parklands Dr., Southport, QLD, 4222, Australia. yaoqi.zhou@griffith.edu.au.ORCID http://orcid.org/0000-0002-9958-5699

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The majority of our human genome transcribes into noncoding RNAs with unknown structures and functions. Obtaining functional clues for noncoding RNAs requires accurate base-pairing or secondary-structure prediction. However, the performance of such predictions by current folding-based algorithms has been stagnated for more than a decade. Here, we propose the use of deep contextual learning for base-pair prediction including those noncanonical and non-nested (pseudoknot) base pairs stabilized by tertiary interactions. Since only [Formula: see text]250 nonredundant, high-resolution RNA structures are available for model training, we utilize transfer learning from a model initially trained with a recent high-quality bpRNA dataset of [Formula: see text]10,000 nonredundant RNAs made available through comparative analysis. The resulting method achieves large, statistically significant improvement in predicting all base pairs, noncanonical and non-nested base pairs in particular. The proposed method (SPOT-RNA), with a freely available server and standalone software, should be useful for improving RNA structure modeling, sequence alignment, and functional annotations.

Indexed as

Neural Networks, ComputerSoftwareAlgorithmsBase PairingComputational BiologyDatabases, GeneticDeep LearningHumansProtein Structure, SecondaryRNARNA, UntranslatedRNARNA, Untranslated

Identifiers

PMID31776342
PMCPMC6881452

What OpenQuestion holds

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LicenceCC BY
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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.