Evidence map›Paper›PMID 35529153›Full record

ArticleRSC advances2019

NCPCDA: network consistency projection for circRNA-disease association prediction.

Guanghui Li, Yingjie Yue, Cheng Liang, Qiu Xiao, Pingjian Ding, Jiawei Luo

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In one paragraph

Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Guanghui LiSchool of Information Engineering, East China Jiaotong University Nanchang 330013 China ghli16@hnu.edu.cn.ORCID https://orcid.org/0000-0001-6531-1166
Yingjie YueSchool of Science, East China Jiaotong University Nanchang 330013 China yueyingjie001@163.com.
Cheng LiangCollege of Information Science and Engineering, Shandong Normal University Jinan 250000 China alcs417@hnu.edu.cn.
Qiu XiaoCollege of Information Science and Engineering, Hunan Normal University Changsha 410081 China hnuyldf@hnu.edu.cn.
Pingjian DingSchool of Computer Science, University of South China Hengyang 421001 China dpjhnu@qq.com.
Jiawei LuoCollege of Computer Science and Electronic Engineering, Hunan University Changsha 410082 China luojiawei@hnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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).

Identifiers

PMID35529153
PMCPMC9073279

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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.