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DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features

BACKGROUND: Circular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures. Compared with the traditional linear RNA, circRNA is more stable and not easily degraded. Many studies have shown that circRNAs are involved in the regulation of various diseases and cancers. Determ...

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Autores principales: Deng, Lei, Lin, Wei, Wang, Jiacheng, Zhang, Jingpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659092/
https://www.ncbi.nlm.nih.gov/pubmed/33183227
http://dx.doi.org/10.1186/s12859-020-03748-3
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author Deng, Lei
Lin, Wei
Wang, Jiacheng
Zhang, Jingpu
author_facet Deng, Lei
Lin, Wei
Wang, Jiacheng
Zhang, Jingpu
author_sort Deng, Lei
collection PubMed
description BACKGROUND: Circular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures. Compared with the traditional linear RNA, circRNA is more stable and not easily degraded. Many studies have shown that circRNAs are involved in the regulation of various diseases and cancers. Determining the functions of circRNAs in mammalian cells is of great significance for revealing their mechanism of action in physiological and pathological processes, diagnosis and treatment of diseases. However, determining the functions of circRNAs on a large scale is a challenging task because of the high experimental costs. RESULTS: In this paper, we present a hierarchical deep learning model, DeepciRGO, which can effectively predict gene ontology functions of circRNAs. We build a heterogeneous network containing circRNA co-expressions, protein–protein interactions and protein–circRNA interactions. The topology features of proteins and circRNAs are calculated using a novel representation learning approach HIN2Vec across the heterogeneous network. Then, a deep multi-label hierarchical classification model is trained with the topology features to predict the biological process function in the gene ontology for each circRNA. In particular, we manually curated a benchmark dataset containing 185 GO annotations for 62 circRNAs, namely, circRNA2GO-62. The DeepciRGO achieves promising performance on the circRNA2GO-62 dataset with a maximum F-measure of 0.412, a recall score of 0.400, and an accuracy of 0.425, which are significantly better than other state-of-the-art RNA function prediction methods. In addition, we demonstrate the considerable potential of integrating multiple interactions and association networks. CONCLUSIONS: DeepciRGO will be a useful tool for accurately annotating circRNAs. The experimental results show that integrating multi-source data can help to improve the predictive performance of DeepciRGO. Moreover, The model also can combine RNA structure and sequence information to further optimize predictive performance.
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spelling pubmed-76590922020-11-13 DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features Deng, Lei Lin, Wei Wang, Jiacheng Zhang, Jingpu BMC Bioinformatics Research Article BACKGROUND: Circular RNAs (circRNAs) are special noncoding RNA molecules with closed loop structures. Compared with the traditional linear RNA, circRNA is more stable and not easily degraded. Many studies have shown that circRNAs are involved in the regulation of various diseases and cancers. Determining the functions of circRNAs in mammalian cells is of great significance for revealing their mechanism of action in physiological and pathological processes, diagnosis and treatment of diseases. However, determining the functions of circRNAs on a large scale is a challenging task because of the high experimental costs. RESULTS: In this paper, we present a hierarchical deep learning model, DeepciRGO, which can effectively predict gene ontology functions of circRNAs. We build a heterogeneous network containing circRNA co-expressions, protein–protein interactions and protein–circRNA interactions. The topology features of proteins and circRNAs are calculated using a novel representation learning approach HIN2Vec across the heterogeneous network. Then, a deep multi-label hierarchical classification model is trained with the topology features to predict the biological process function in the gene ontology for each circRNA. In particular, we manually curated a benchmark dataset containing 185 GO annotations for 62 circRNAs, namely, circRNA2GO-62. The DeepciRGO achieves promising performance on the circRNA2GO-62 dataset with a maximum F-measure of 0.412, a recall score of 0.400, and an accuracy of 0.425, which are significantly better than other state-of-the-art RNA function prediction methods. In addition, we demonstrate the considerable potential of integrating multiple interactions and association networks. CONCLUSIONS: DeepciRGO will be a useful tool for accurately annotating circRNAs. The experimental results show that integrating multi-source data can help to improve the predictive performance of DeepciRGO. Moreover, The model also can combine RNA structure and sequence information to further optimize predictive performance. BioMed Central 2020-11-12 /pmc/articles/PMC7659092/ /pubmed/33183227 http://dx.doi.org/10.1186/s12859-020-03748-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Deng, Lei
Lin, Wei
Wang, Jiacheng
Zhang, Jingpu
DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title_full DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title_fullStr DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title_full_unstemmed DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title_short DeepciRGO: functional prediction of circular RNAs through hierarchical deep neural networks using heterogeneous network features
title_sort deepcirgo: functional prediction of circular rnas through hierarchical deep neural networks using heterogeneous network features
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7659092/
https://www.ncbi.nlm.nih.gov/pubmed/33183227
http://dx.doi.org/10.1186/s12859-020-03748-3
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