Evidence map›Paper›PMID 39701957›Full record

ArticleBMC bioinformatics2024

Prediction of miRNA-disease associations based on PCA and cascade forest.

Chuanlei Zhang, Yubo Li, Yinglun Dong, Wei Chen, Changqing Yu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
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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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Chuanlei ZhangArtificial Intelligence, Tianjin University of Science and Technology, Tianjin, 300457, China.
Yubo LiArtificial Intelligence, Tianjin University of Science and Technology, Tianjin, 300457, China.
Yinglun DongArtificial Intelligence, Tianjin University of Science and Technology, Tianjin, 300457, China.
Wei ChenComputer Science, China University of Mining and Technology, Xuzhou, 221116, China.
Changqing YuElectronic Information, Xijing University, Xi'an, 710123, China. xaycq@163.com.

Funding

National Natural Science Foundation of China 62172338
6 · The paper itself

Abstract

backgroundAs a key non-coding RNA molecule, miRNA profoundly affects gene expression regulation and connects to the pathological processes of several kinds of human diseases. However, conventional experimental methods for validating miRNA-disease associations are laborious. Consequently, the development of efficient and reliable computational prediction models is crucial for the identification and validation of these associations.

resultsIn this research, we developed the PCACFMDA method to predict the potential associations between miRNAs and diseases. To construct a multidimensional feature matrix, we consider the fusion similarities of miRNA and disease and miRNA-disease pairs. We then use principal component analysis(PCA) to reduce data complexity and extract low-dimensional features. Subsequently, a tuned cascade forest is used to mine the features and output prediction scores deeply. The results of the 5-fold cross-validation using the HMDD v2.0 database indicate that the PCACFMDA algorithm achieved an AUC of 98.56%. Additionally, we perform case studies on breast, esophageal and lung neoplasms. The findings revealed that the top 50 miRNAs most strongly linked to each disease have been validated.

conclusionsBased on PCA and optimized cascade forests, we propose the PCACFMDA model for predicting undiscovered miRNA-disease associations. The experimental results demonstrate superior prediction performance and commendable stability. Consequently, the PCACFMDA is a potent instrument for in-depth exploration of miRNA-disease associations.

Indexed as

AlgorithmsMicroRNAsPrincipal Component AnalysisBreast NeoplasmsComputational BiologyEsophageal NeoplasmsGenetic Predisposition to DiseaseHumansLung NeoplasmsMicroRNAsCascade forestEnsemble learningmiRNA-disease AssociationPCA

Identifiers

PMID39701957
PMCPMC11660965

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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.