Evidence map›Paper›PMID 40874819›Full record

ArticleBriefings in bioinformatics2025

BBANsh: a deep learning architecture based on BERT and bilinear attention networks to identify potent shRNA.

Yuanting Chen, Long Chen, Xinxin Yu, Weihua Li, Yun Tang, Guixia Liu

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Yuanting ChenShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Long ChenShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Xinxin YuShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Weihua LiShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Yun TangShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.ORCID 0000-0003-2340-1109
Guixia LiuShanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.ORCID 0000-0001-9648-844X

Funding

National Natural Science Foundation of China 82273858National Natural Science Foundation of China U23A20530Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism (Shanghai Municipal Education Commission)
6 · The paper itself

Abstract

RNA interference (RNAi) is a technique for precisely silencing the expression of specific genes by means of small RNA molecules and is essential in functional genomics. Among the commonly used RNAi molecules, short hairpin RNAs (shRNAs) exhibit advantages over small interfering RNAs, including longer half-life, comparable silencing efficiency, fewer off-target effects, and greater safety. However, traditional screening of potent shRNAs is costly and time-consuming. Advances in big data and artificial intelligence have enabled computational methods to significantly accelerate shRNA design and prediction. In this study, we propose BBANsh, a new shRNA prediction model based on bidirectional encoder representation from transformers (BERT) and bilinear attention network (BAN). We comprehensively evaluate the performance of BBANsh against traditional feature-based models, various feature fusion methods, and existing shRNA prediction models. The BBANsh has achieved an area under the precision-recall curve of 0.951 on five-cross validation and a prediction accuracy of 0.896 on a new external validation set, highlighting its superior predictive performance. Ablation experiments validate the significant contributions of BERT and BAN to model performance. The visualization of internal feature representations intuitively demonstrates the effectiveness of the feature fusion strategy of BBANsh. Furthermore, the attentional analysis reveals that nucleotides near the 5' end have the greatest impact on model predictions, highlighting sequence characteristics of potent shRNAs. Overall, BBANsh provides an efficient and reliable tool for shRNA prediction, which can offer valuable support for researchers in the precise selection and design of shRNA.

Indexed as

Computational BiologyDeep LearningRNA InterferenceRNA, Small InterferingAlgorithmsHumansNeural Networks, ComputerRNA, Small InterferingBERTbilinear attention networkshRNA prediction

Identifiers

PMID40874819
PMCPMC12392269

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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.