Evidence map›Paper›PMID 39503523›Full record

ArticleBriefings in bioinformatics2024

siRNADiscovery: a graph neural network for siRNA efficacy prediction via deep RNA sequence analysis.

Rongzhuo Long, Ziyu Guo, Da Han, Boxiang Liu, Xudong Yuan, Guangyong Chen, Pheng-Ann Heng, Liang Zhang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

8 authors.

Rongzhuo LongSchool of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University, 211198, Nanjing, China.ORCID 0000-0003-3755-5491
Ziyu GuoDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Central Ave, Hong Kong SAR, China.ORCID 0000-0001-9606-9691
Da HanInstitute of Molecular Medicine (IMM) and Department of Laboratory Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, 200240, Shanghai, China.ORCID 0000-0002-0804-2964
Boxiang LiuDepartment of Pharmacy, Faculty of Science, National University of Singapore, Singapore, 117543, Singapore.ORCID 0000-0002-2595-4463
Xudong YuanACON Pharmaceuticals, 2557 Route 130 S, Ste 3, Cranbury, NJ 08512, USA.ORCID 0000-0002-8683-4297
Guangyong ChenZhejiang Lab, Ke Chuang Avenue, 311121, Zhejiang, China.ORCID 0000-0002-5892-8608
Pheng-Ann HengDepartment of Computer Science and Engineering, The Chinese University of Hong Kong, Central Ave, Hong Kong SAR, China.ORCID 0000-0003-3055-5034
Liang ZhangHangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, 310022, Hangzhou, Zhejiang, China.ORCID 0000-0003-1146-7848

Funding

Hong Kong Innovation and Technology Fund ITS/241/21National Natural Science Foundation of China 32470995,62376254National Natural Science Foundation of China & the Bill & Melinda Gates Foundation 72361127503
6 · The paper itself

Abstract

The clinical adoption of small interfering RNAs (siRNAs) has prompted the development of various computational strategies for siRNA design, from traditional data analysis to advanced machine learning techniques. However, previous studies have inadequately considered the full complexity of the siRNA silencing mechanism, neglecting critical elements such as siRNA positioning on mRNA, RNA base-pairing probabilities, and RNA-AGO2 interactions, thereby limiting the insight and accuracy of existing models. Here, we introduce siRNADiscovery, a Graph Neural Network (GNN) framework that leverages both non-empirical and empirical rule-based features of siRNA and mRNA to effectively capture the complex dynamics of gene silencing. On multiple internal datasets, siRNADiscovery achieves state-of-the-art performance. Significantly, siRNADiscovery also outperforms existing methodologies in in vitro studies and on an externally validated dataset. Additionally, we develop a new data-splitting methodology that addresses the data leakage issue, a frequently overlooked problem in previous studies, ensuring the robustness and stability of our model under various experimental settings. Through rigorous testing, siRNADiscovery has demonstrated remarkable predictive accuracy and robustness, making significant contributions to the field of gene silencing. Furthermore, our approach to redefining data-splitting standards aims to set new benchmarks for future research in the domain of predictive biological modeling for siRNA.

Indexed as

Neural Networks, ComputerRNA, Small InterferingAlgorithmsComputational BiologyGene SilencingHumansRNA InterferenceRNA, MessengerSequence Analysis, RNARNA, MessengerRNA, Small Interferingdeep learninggene silencing efficacygraph neural networkRNA sequence analysissiRNA efficacy prediction

Identifiers

PMID39503523
PMCPMC11539000

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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.