Evidence map›Paper›PMID 27517318›Full record

ArticleOncotarget2016

IRWRLDA: improved random walk with restart for lncRNA-disease association prediction.

Xing Chen, Zhu-Hong You, Gui-Ying Yan, Dun-Wei Gong

Abstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 100 papers.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

100 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xing ChenSchool of Information and Electrical Engineering, China University of Mining and Technology, Xuzhou, 221116, China.
Zhu-Hong YouSchool of Computer Science and Technology, China University of Mining and Technology, Xuzhou, 221116, China.
Gui-Ying YanAcademy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100190, China.
Dun-Wei GongSchool of Information and Electrical Engineering, China University of Mining and Technology, Xuzhou, 221116, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, accumulating evidences have shown that the dysregulations of lncRNAs are associated with a wide range of human diseases. It is necessary and feasible to analyze known lncRNA-disease associations, predict potential lncRNA-disease associations, and provide the most possible lncRNA-disease pairs for experimental validation. Considering the limitations of traditional Random Walk with Restart (RWR), the model of Improved Random Walk with Restart for LncRNA-Disease Association prediction (IRWRLDA) was developed to predict novel lncRNA-disease associations by integrating known lncRNA-disease associations, disease semantic similarity, and various lncRNA similarity measures. The novelty of IRWRLDA lies in the incorporation of lncRNA expression similarity and disease semantic similarity to set the initial probability vector of the RWR. Therefore, IRWRLDA could be applied to diseases without any known related lncRNAs. IRWRLDA significantly improved previous classical models with reliable AUCs of 0.7242 and 0.7872 in two known lncRNA-disease association datasets downloaded from the lncRNADisease database, respectively. Further case studies of colon cancer and leukemia were implemented for IRWRLDA and 60% of lncRNAs in the top 10 prediction lists have been confirmed by recent experimental reports.

Indexed as

AlgorithmsArea Under CurveColonic NeoplasmsComputational BiologyComputer SimulationDatabases, GeneticGenetic Predisposition to DiseaseHumansLeukemiaModels, StatisticalNormal DistributionProbabilityReproducibility of ResultsRNA, Long NoncodingRNA, Long NoncodingcancerdiseaselncRNAsrandom walk with restart

Identifiers

PMID27517318
PMCPMC5295400

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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.