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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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). |
format | Online Article Text |
id | pubmed-9073279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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