Evidence map›Paper›PMID 31921290›Full record

ArticleFrontiers in genetics2019

Identifying Potential miRNAs-Disease Associations With Probability Matrix Factorization.

Junlin Xu, Lijun Cai, Bo Liao, Wen Zhu, Peng Wang, Yajie Meng, Jidong Lang, Geng Tian, Jialiang Yang

Abstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

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0cells of the map it votes in
22citing papers in PubMed
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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

22 citing papers in PubMed.

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  6. Hessian RegularizedInterdisciplinary sciences, computational life sciences · 2024
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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Junlin XuCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, China.
Lijun CaiCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, China.
Bo LiaoSchool of Mathematics and Statistics, Hainan Normal University, Haikou, China.
Wen ZhuCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, China.
Peng WangCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, China.
Yajie MengCollege of Computer Science and Electronic Engineering, Hunan University, Changsha, China.
Jidong LangDepartment of Science, Geneis Beijing Co., Ltd., Beijing, China.
Geng TianDepartment of Science, Geneis Beijing Co., Ltd., Beijing, China.
Jialiang YangSchool of Mathematics and Statistics, Hainan Normal University, Haikou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, miRNAs have been verified to play an irreplaceable role in biological processes associated with human disease. Discovering potential disease-related miRNAs helps explain the underlying pathogenesis of the disease at the molecular level. Given the high cost and labor intensity of biological experiments, computational predictions will be an indispensable alternative. Therefore, we design a new model called probability matrix factorization (PMFMDA). Specifically, we first integrate miRNA and disease similarity. Next, the known association matrix and integrated similarity matrix are utilized to construct a probability matrix factorization algorithm to identify potentially relevant miRNAs for disease. We find that PMFMDA achieves reliable performance in the frameworks of global leave-one-out cross validation (LOOCV) and 5-fold cross validation (AUCs are 0.9237 and 0.9187, respectively) in the HMDD (V2.0) dataset, significantly outperforming a few state-of-the-art methods including CMFMDA, IMCMDA, NCPMDA, RLSMDA, and RWRMDA. In addition, case studies show that PMFMDA has good predictive performance for new associations, and the evidence can be identified by literature mining.

Indexed as

association predictiondiseasesmiRNAsprobabilistic matrix factorizationreceiver operating characteristic curve (ROC)

Identifiers

PMID31921290
PMCPMC6918542

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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.