Evidence map›Paper›PMID 35558942›Full record

ArticleRSC advances2018

A novel information diffusion method based on network consistency for identifying disease related microRNAs.

Min Chen, Yan Peng, Ang Li, Zejun Li, Yingwei Deng, Wenhua Liu, Bo Liao, Chengqiu Dai

Abstract read
In one paragraph

Article in RSC advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Min ChenCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.ORCID https://orcid.org/0000-0002-7019-9102
Yan PengCollege of International Communication, Hunan Institute of Technology 421002 Hengyang China.
Ang LiCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.
Zejun LiCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.
Yingwei DengCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.
Wenhua LiuCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.
Bo LiaoCollege of Information Science and Engineering, Hunan University Changsha 410082 China dragonbw@163.com.
Chengqiu DaiCollege of Computer Science and Technology, Hunan Institute of Technology 421002 Hengyang China liang@hnit.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The abnormal expression of miRNAs is directly related to the development of human diseases. Predicting the potential candidate miRNAs associated with diseases can contribute to the detection, diagnosis, treatment and prevention of human complex diseases. The effective inference of the calculation method of the relationship between miRNAs and diseases is an effective supplement to biological experiments. It is of great help in the prevention, treatment and prognosis of complex diseases. This paper proposes a novel information diffusion method based on network consistency (IDNC) for identifying disease related microRNAs. The model first synthesizes the miRNA family information and the miRNA function similarity to reconstruct the miRNA network, and reconstruct the disease network by using the known disease and miRNA-related information and the semantic score between diseases. Then the global similarity of the two networks is obtained by using the Laplacian score of graphs. The global similarity score is a measure of the similarity between diseases and miRNAs. The disease-miRNA relation network was reconstructed by integrating the global similarity relation. The network consistency diffusion seed is then obtained by combining the global similarity network with the reconstructed disease-miRNA association network. Thereafter, the stable diffusion spectrum is generated as the prediction score by using the restarted random walk algorithm. The AUC value obtained by performing the LOOCV in the gold benchmark dataset is 0.8814. The AUC value obtained by performing the LOOCV in the predictive dataset is 0.9512. Compared with other frontier methods, our method has higher accuracy, which is further illustrated by case studies of breast neoplasms and colon neoplasms to prove that IDNC is valuable.

Identifiers

PMID35558942
PMCPMC9088870

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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.