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NCPCDA: network consistency projection for circRNA–disease association prediction

A growing body of evidence indicates that circular RNAs (circRNAs) play a pivotal role in various biological processes and have a close association with the initiation and progression of diseases. Moreover, circRNAs are considered as promising biomarkers for disease diagnosis owing to their characte...

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Autores principales: Li, Guanghui, Yue, Yingjie, Liang, Cheng, Xiao, Qiu, Ding, Pingjian, Luo, Jiawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073279/
https://www.ncbi.nlm.nih.gov/pubmed/35529153
http://dx.doi.org/10.1039/c9ra06133a
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author Li, Guanghui
Yue, Yingjie
Liang, Cheng
Xiao, Qiu
Ding, Pingjian
Luo, Jiawei
author_facet Li, Guanghui
Yue, Yingjie
Liang, Cheng
Xiao, Qiu
Ding, Pingjian
Luo, Jiawei
author_sort Li, Guanghui
collection PubMed
description A growing body of evidence indicates that circular RNAs (circRNAs) play a pivotal role in various biological processes and have a close association with the initiation and progression of diseases. Moreover, circRNAs are considered as promising biomarkers for disease diagnosis owing to their characteristics of conservation, stability and universality. Inferring disease–circRNA relationships will contribute to the understanding of disease pathology. However, it is costly and laborious to discover novel disease–circRNA interactions by wet-lab experiments, and few computational methods have been devoted to predicting potential circRNAs for diseases. Here, we advance a computational method (NCPCDA) to identify novel circRNA–disease associations based on network consistency projection. For starters, we make use of multi-view similarity data, including circRNA functional similarity, disease semantic similarity, and association profile similarity, to construct the integrated circRNA similarity and disease similarity. Then, we project circRNA space and disease space on the circRNA–disease interaction network, respectively. Finally, we can obtain the predicted circRNA–disease association score matrix by combining the above two space projection scores. Simulation results show that NCPCDA can efficiently infer disease–circRNA relationships with high accuracy, obtaining AUCs of 0.9541 and 0.9201 in leave-one-out cross validation and five-fold cross validation, respectively. Furthermore, case studies also suggest that NCPCDA is promising for discovering new disease–circRNA interactions. The NCPCDA dataset and code, as well as the detailed readme file for our code, can be downloaded from Github (https://github.com/ghli16/NNCPCD).
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spelling pubmed-90732792022-05-06 NCPCDA: network consistency projection for circRNA–disease association prediction Li, Guanghui Yue, Yingjie Liang, Cheng Xiao, Qiu Ding, Pingjian Luo, Jiawei RSC Adv Chemistry A growing body of evidence indicates that circular RNAs (circRNAs) play a pivotal role in various biological processes and have a close association with the initiation and progression of diseases. Moreover, circRNAs are considered as promising biomarkers for disease diagnosis owing to their characteristics of conservation, stability and universality. Inferring disease–circRNA relationships will contribute to the understanding of disease pathology. However, it is costly and laborious to discover novel disease–circRNA interactions by wet-lab experiments, and few computational methods have been devoted to predicting potential circRNAs for diseases. Here, we advance a computational method (NCPCDA) to identify novel circRNA–disease associations based on network consistency projection. For starters, we make use of multi-view similarity data, including circRNA functional similarity, disease semantic similarity, and association profile similarity, to construct the integrated circRNA similarity and disease similarity. Then, we project circRNA space and disease space on the circRNA–disease interaction network, respectively. Finally, we can obtain the predicted circRNA–disease association score matrix by combining the above two space projection scores. Simulation results show that NCPCDA can efficiently infer disease–circRNA relationships with high accuracy, obtaining AUCs of 0.9541 and 0.9201 in leave-one-out cross validation and five-fold cross validation, respectively. Furthermore, case studies also suggest that NCPCDA is promising for discovering new disease–circRNA interactions. The NCPCDA dataset and code, as well as the detailed readme file for our code, can be downloaded from Github (https://github.com/ghli16/NNCPCD). The Royal Society of Chemistry 2019-10-16 /pmc/articles/PMC9073279/ /pubmed/35529153 http://dx.doi.org/10.1039/c9ra06133a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Guanghui
Yue, Yingjie
Liang, Cheng
Xiao, Qiu
Ding, Pingjian
Luo, Jiawei
NCPCDA: network consistency projection for circRNA–disease association prediction
title NCPCDA: network consistency projection for circRNA–disease association prediction
title_full NCPCDA: network consistency projection for circRNA–disease association prediction
title_fullStr NCPCDA: network consistency projection for circRNA–disease association prediction
title_full_unstemmed NCPCDA: network consistency projection for circRNA–disease association prediction
title_short NCPCDA: network consistency projection for circRNA–disease association prediction
title_sort ncpcda: network consistency projection for circrna–disease association prediction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073279/
https://www.ncbi.nlm.nih.gov/pubmed/35529153
http://dx.doi.org/10.1039/c9ra06133a
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