Evidence map›Paper›PMID 31455028›Full record

ArticleCells2019

A Novel Computational Model for Predicting microRNA-Disease Associations Based on Heterogeneous Graph Convolutional Networks.

Chunyan Li, Hongju Liu, Qian Hu, Jinlong Que, Junfeng Yao

Abstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

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

21 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

5 authors.

Chunyan LiSchool of Informatics, Xiamen University, Xiamen 361005, China.
Hongju LiuCollege of Information Technology and Computer Science, University of the Cordilleras, Baguio 2600, Philippines.
Qian HuSchool of Informatics, Xiamen University, Xiamen 361005, China.
Jinlong QueSchool of Informatics, Xiamen University, Xiamen 361005, China.
Junfeng YaoSchool of Informatics, Xiamen University, Xiamen 361005, China. yao0010@xmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identifying the interactions between disease and microRNA (miRNA) can accelerate drugs development, individualized diagnosis, and treatment for various human diseases. However, experimental methods are time-consuming and costly. So computational approaches to predict latent miRNA-disease interactions are eliciting increased attention. But most previous studies have mainly focused on designing complicated similarity-based methods to predict latent interactions between miRNAs and diseases. In this study, we propose a novel computational model, termed heterogeneous graph convolutional network for miRNA-disease associations (HGCNMDA), which is based on known human protein-protein interaction (PPI) and integrates four biological networks: miRNA-disease, miRNA-gene, disease-gene, and PPI network. HGCNMDA achieved reliable performance using leave-one-out cross-validation (LOOCV). HGCNMDA is then compared to three state-of-the-art algorithms based on five-fold cross-validation. HGCNMDA achieves an AUC of 0.9626 and an average precision of 0.9660, respectively, which is ahead of other competitive algorithms. We further analyze the top-10 unknown interactions between miRNA and disease. In summary, HGCNMDA is a useful computational model for predicting miRNA-disease interactions.

Indexed as

Genetic Predisposition to DiseaseAlgorithmsArea Under CurveComputational BiologyComputer SimulationDatabases, GeneticGenetic Association StudiesHumansMicroRNAsProtein Interaction MapsMicroRNAsconvolution networkcross validationdiseasegraphheterogeneousmicroRNAnegative sampling

Identifiers

PMID31455028
PMCPMC6769654

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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.