DeepCMI: a graph-based model for accurate prediction of circRNA-miRNA interactions with multiple information.

IF 2.5 3区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Briefings in Functional Genomics Pub Date : 2024-05-15 DOI:10.1093/bfgp/elad030
Yue-Chao Li, Zhu-Hong You, Chang-Qing Yu, Lei Wang, Lun Hu, Peng-Wei Hu, Yan Qiao, Xin-Fei Wang, Yu-An Huang
{"title":"DeepCMI: a graph-based model for accurate prediction of circRNA-miRNA interactions with multiple information.","authors":"Yue-Chao Li, Zhu-Hong You, Chang-Qing Yu, Lei Wang, Lun Hu, Peng-Wei Hu, Yan Qiao, Xin-Fei Wang, Yu-An Huang","doi":"10.1093/bfgp/elad030","DOIUrl":null,"url":null,"abstract":"<p><p>Recently, the role of competing endogenous RNAs in regulating gene expression through the interaction of microRNAs has been closely associated with the expression of circular RNAs (circRNAs) in various biological processes such as reproduction and apoptosis. While the number of confirmed circRNA-miRNA interactions (CMIs) continues to increase, the conventional in vitro approaches for discovery are expensive, labor intensive, and time consuming. Therefore, there is an urgent need for effective prediction of potential CMIs through appropriate data modeling and prediction based on known information. In this study, we proposed a novel model, called DeepCMI, that utilizes multi-source information on circRNA/miRNA to predict potential CMIs. Comprehensive evaluations on the CMI-9905 and CMI-9589 datasets demonstrated that DeepCMI successfully infers potential CMIs. Specifically, DeepCMI achieved AUC values of 90.54% and 94.8% on the CMI-9905 and CMI-9589 datasets, respectively. These results suggest that DeepCMI is an effective model for predicting potential CMIs and has the potential to significantly reduce the need for downstream in vitro studies. To facilitate the use of our trained model and data, we have constructed a computational platform, which is available at http://120.77.11.78/DeepCMI/. The source code and datasets used in this work are available at https://github.com/LiYuechao1998/DeepCMI.</p>","PeriodicalId":55323,"journal":{"name":"Briefings in Functional Genomics","volume":" ","pages":"276-285"},"PeriodicalIF":2.5000,"publicationDate":"2024-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Briefings in Functional Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bfgp/elad030","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Recently, the role of competing endogenous RNAs in regulating gene expression through the interaction of microRNAs has been closely associated with the expression of circular RNAs (circRNAs) in various biological processes such as reproduction and apoptosis. While the number of confirmed circRNA-miRNA interactions (CMIs) continues to increase, the conventional in vitro approaches for discovery are expensive, labor intensive, and time consuming. Therefore, there is an urgent need for effective prediction of potential CMIs through appropriate data modeling and prediction based on known information. In this study, we proposed a novel model, called DeepCMI, that utilizes multi-source information on circRNA/miRNA to predict potential CMIs. Comprehensive evaluations on the CMI-9905 and CMI-9589 datasets demonstrated that DeepCMI successfully infers potential CMIs. Specifically, DeepCMI achieved AUC values of 90.54% and 94.8% on the CMI-9905 and CMI-9589 datasets, respectively. These results suggest that DeepCMI is an effective model for predicting potential CMIs and has the potential to significantly reduce the need for downstream in vitro studies. To facilitate the use of our trained model and data, we have constructed a computational platform, which is available at http://120.77.11.78/DeepCMI/. The source code and datasets used in this work are available at https://github.com/LiYuechao1998/DeepCMI.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
DeepCMI:基于图的模型,可准确预测具有多种信息的 circRNA-miRNA 相互作用。
最近,竞争性内源 RNA 通过 microRNAs 的相互作用在调节基因表达方面的作用与循环 RNAs(circRNAs)在繁殖和凋亡等各种生物过程中的表达密切相关。虽然已证实的环状 RNA-miRNA 相互作用(CMIs)的数量在不断增加,但传统的体外发现方法成本高、劳动强度大且耗时。因此,迫切需要通过适当的数据建模和基于已知信息的预测来有效预测潜在的 CMIs。在这项研究中,我们提出了一种名为 DeepCMI 的新型模型,该模型利用 circRNA/miRNA 的多源信息来预测潜在的 CMIs。在 CMI-9905 和 CMI-9589 数据集上进行的综合评估表明,DeepCMI 成功地推断出了潜在的 CMI。具体来说,DeepCMI 在 CMI-9905 和 CMI-9589 数据集上的 AUC 值分别达到了 90.54% 和 94.8%。这些结果表明,DeepCMI 是预测潜在 CMI 的有效模型,并有可能大大减少下游体外研究的需要。为了方便使用我们训练有素的模型和数据,我们构建了一个计算平台,可在 http://120.77.11.78/DeepCMI/ 上查阅。这项工作中使用的源代码和数据集可在 https://github.com/LiYuechao1998/DeepCMI 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Briefings in Functional Genomics
Briefings in Functional Genomics BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
6.30
自引率
2.50%
发文量
37
审稿时长
6-12 weeks
期刊介绍: Briefings in Functional Genomics publishes high quality peer reviewed articles that focus on the use, development or exploitation of genomic approaches, and their application to all areas of biological research. As well as exploring thematic areas where these techniques and protocols are being used, articles review the impact that these approaches have had, or are likely to have, on their field. Subjects covered by the Journal include but are not restricted to: the identification and functional characterisation of coding and non-coding features in genomes, microarray technologies, gene expression profiling, next generation sequencing, pharmacogenomics, phenomics, SNP technologies, transgenic systems, mutation screens and genotyping. Articles range in scope and depth from the introductory level to specific details of protocols and analyses, encompassing bacterial, fungal, plant, animal and human data. The editorial board welcome the submission of review articles for publication. Essential criteria for the publication of papers is that they do not contain primary data, and that they are high quality, clearly written review articles which provide a balanced, highly informative and up to date perspective to researchers in the field of functional genomics.
期刊最新文献
Systematic analysis of the transcriptional landscape of melanoma reveals drug-target expression plasticity. Exploring the impact of N4-acetylcytidine modification in RNA on non-neoplastic disease: unveiling its role in pathogenesis and therapeutic opportunities. Crosstalk between genomic variants and DNA methylation in FLT3 mutant acute myeloid leukemia. Beyond the hype: using AI, big data, wearable devices, and the internet of things for high-throughput livestock phenotyping. Environmental community transcriptomics: strategies and struggles.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1