Evidence map›Paper›PMID 34461870›Full record

ArticleBMC medical informatics and decision making2021

Efficient framework for predicting MiRNA-disease associations based on improved hybrid collaborative filtering.

Ru Nie, Zhengwei Li, Zhu-Hong You, Wenzheng Bao, Jiashu Li

Open access · goldAbstract read
In one paragraph

Article in BMC medical informatics and decision making, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors at 4 institutions in 1 country.

Ru Nie *Engineering Research Center of Mine Digitalization of Ministry of Education, China University of Mining and Technology, Xuzhou, 221116, China.
Zhengwei Li *Engineering Research Center of Mine Digitalization of Ministry of Education, China University of Mining and Technology, Xuzhou, 221116, China. zwli@cumt.edu.cn.ORCID 0000-0003-1644-1006
Zhu-Hong YouSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China. zhuhongyou@gmail.com.
Wenzheng BaoSchool of Information Engineering, Xuzhou University of Technology, Xuzhou, 221018, China.
Jiashu LiEngineering Research Center of Mine Digitalization of Ministry of Education, China University of Mining and Technology, Xuzhou, 221116, China.
China University of Mining and Technology · CNNorthwestern Polytechnical University · CNTongji University · CNXuzhou University of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccumulating studies indicates that microRNAs (miRNAs) play vital roles in the process of development and progression of many human complex diseases. However, traditional biochemical experimental methods for identifying disease-related miRNAs cost large amount of time, manpower, material and financial resources.

methodsIn this study, we developed a framework named hybrid collaborative filtering for miRNA-disease association prediction (HCFMDA) by integrating heterogeneous data, e.g., miRNA functional similarity, disease semantic similarity, known miRNA-disease association networks, and Gaussian kernel similarity of miRNAs and diseases. To capture the intrinsic interaction patterns embedded in the sparse association matrix, we prioritized the predictive score by fusing three types of information: similar disease associations, similar miRNA associations, and similar disease-miRNA associations. Meanwhile, singular value decomposition was adopted to reduce the impact of noise and accelerate predictive speed.

resultsWe then validated HCFMDA with leave-one-out cross-validation (LOOCV) and two types of case studies. In the LOOCV, we achieved 0.8379 of AUC (area under the curve). To evaluate the performance of HCFMDA on real diseases, we further implemented the first type of case validation over three important human diseases: Colon Neoplasms, Esophageal Neoplasms and Prostate Neoplasms. As a result, 44, 46 and 44 out of the top 50 predicted disease-related miRNAs were confirmed by experimental evidence. Moreover, the second type of case validation on Breast Neoplasms indicates that HCFMDA could also be applied to predict potential miRNAs towards those diseases without any known associated miRNA.

conclusionsThe satisfactory prediction performance demonstrates that our model could serve as a reliable tool to guide the following research for identifying candidate miRNAs associated with human diseases.

Indexed as

Computational BiologyMicroRNAsAlgorithmsGenetic Predisposition to DiseaseHumansNeoplasmsMicroRNAsHeterogeneous dataHybrid collaborative filteringmiRNA-disease association predictionSingular value decomposition

Identifiers

PMID34461870
PMCPMC8406577
OpenAlexW3198293327

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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.