Evidence map›Paper›PMID 29272076›Full record

ArticleJournal of cellular and molecular medicine2018

GIMDA: Graphlet interaction-based MiRNA-disease association prediction.

Xing Chen, Na-Na Guan, Jian-Qiang Li, Gui-Ying Yan

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

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0cells of the map it votes in
17citing 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

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Xing ChenSchool of Information and Control Engineering, China University of Mining and Technology, Xuzhou, China.ORCID 0000-0001-9028-5342
Na-Na GuanCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, China.
Jian-Qiang LiCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, China.
Gui-Ying YanAcademy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) have been confirmed to be closely related to various human complex diseases by many experimental studies. It is necessary and valuable to develop powerful and effective computational models to predict potential associations between miRNAs and diseases. In this work, we presented a prediction model of Graphlet Interaction for MiRNA-Disease Association prediction (GIMDA) by integrating the disease semantic similarity, miRNA functional similarity, Gaussian interaction profile kernel similarity and the experimentally confirmed miRNA-disease associations. The related score of a miRNA to a disease was calculated by measuring the graphlet interactions between two miRNAs or two diseases. The novelty of GIMDA lies in that we used graphlet interaction to analyse the complex relationships between two nodes in a graph. The AUCs of GIMDA in global and local leave-one-out cross-validation (LOOCV) turned out to be 0.9006 and 0.8455, respectively. The average result of five-fold cross-validation reached to 0.8927 ± 0.0012. In case study for colon neoplasms, kidney neoplasms and prostate neoplasms based on the database of HMDD V2.0, 45, 45, 41 of the top 50 potential miRNAs predicted by GIMDA were validated by dbDEMC and miR2Disease. Additionally, in the case study of new diseases without any known associated miRNAs and the case study of predicting potential miRNA-disease associations using HMDD V1.0, there were also high percentages of top 50 miRNAs verified by the experimental literatures.

Indexed as

Gene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseModels, StatisticalAgedAlgorithmsArea Under CurveColonic NeoplasmsComputational BiologyHumansKidney NeoplasmsMaleMicroRNAsMiddle AgedProstatic NeoplasmsMicroRNAsdiseasegraphlet interactionmiRNAmiRNA-disease association

Identifiers

PMID29272076
PMCPMC5824414

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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.