Evidence map›Paper›PMID 32974293›Full record

ArticleFrontiers in bioengineering and biotechnology2020

Heterogeneous Graph Convolutional Networks and Matrix Completion for miRNA-Disease Association Prediction.

Rongxiang Zhu, Chaojie Ji, Yingying Wang, Yunpeng Cai, Hongyan Wu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 38% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

4 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Rongxiang ZhuJoint Engineering Research Center for Health Big Data Intelligent Analysis Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Chaojie JiJoint Engineering Research Center for Health Big Data Intelligent Analysis Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Yingying WangDepartment of Neurology and Stroke Center, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Yunpeng CaiJoint Engineering Research Center for Health Big Data Intelligent Analysis Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Hongyan WuJoint Engineering Research Center for Health Big Data Intelligent Analysis Technology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Shenzhen Institutes of Advanced Technology · CNFirst Affiliated Hospital of Jinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the cost and complexity of biological experiments, many computational methods have been proposed to predict potential miRNA-disease associations by utilizing known miRNA-disease associations and other related information. However, there are some challenges for these computational methods. First, the relationships between miRNAs and diseases are complex. The computational network should consider the local and global influence of neighborhoods from the network. Furthermore, predicting disease-related miRNAs without any known associations is also very important. This study presents a new computational method that constructs a heterogeneous network composed of a miRNA similarity network, disease similarity network, and known miRNA-disease association network. The miRNA similarity considers the miRNAs and their possible families and clusters. The information of each node in heterogeneous network is obtained by aggregating neighborhood information with graph convolutional networks (GCNs), which can pass the information of a node to its intermediate and distant neighbors. Disease-related miRNAs with no known associations can be predicted with the reconstructed heterogeneous matrix. We apply 5-fold cross-validation, leave-one-disease-out cross-validation, and global and local leave-one-out cross-validation to evaluate our method. The corresponding areas under the curves (AUCs) are 0.9616, 0.9946, 0.9656, and 0.9532, confirming that our approach significantly outperforms the state-of-the-art methods. Case studies show that this approach can effectively predict new diseases without any known miRNAs.

Indexed as

association predictionGCNsheterogeneous graphmatrix completionmiRNA disease

Identifiers

PMID32974293
PMCPMC7468400
OpenAlexW3080991592

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.