Evidence map›Paper›PMID 33183227›Full record

ArticleBMC bioinformatics2020

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

Lei Deng, Wei Lin, Jiacheng Wang, Jingpu Zhang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Lei DengSchool of Computer Science and Engineering, Central South University, Changsha, 410075, China.
Wei LinSchool of Computer Science and Engineering, Central South University, Changsha, 410075, China.
Jiacheng WangSchool of Computer Science and Engineering, Central South University, Changsha, 410075, China.
Jingpu ZhangSchool of Computer and Data Science, Henan University of Urban Construction, Pingdingshan, 467000, China. zhangjp@csu.edu.cn.ORCID http://orcid.org/0000-0002-8006-747X

Funding

Foundation of Henan Educational Committee (CN) 20B520005National Natural Science Foundation of China 61672541National Natural Science Foundation of China 61972422
6 · The paper itself

Abstract

backgroundCircular 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.

resultsIn 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.

conclusionsDeepciRGO 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.

Indexed as

Neural Networks, ComputerCell Line, TumorCell MovementCell ProliferationDNA HelicasesGene OntologyGenetic LociHumansProtein Interaction MapsRNA, CircularUbiquitin-Protein LigasesDNA HelicasesRNA, CircularSHPRH protein, humanUbiquitin-Protein LigasesGene ontologyHIN2VecMulti-label hierarchical classificationRepresentation learning

Identifiers

PMID33183227
PMCPMC7659092

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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.