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Updated: Jan 19, 2026

Generation and 3-Dimensional Quantitation of Arterial Lesions in Mice Using Optical Projection Tomography
Published on: May 26, 2015
Predicting miRNA-Disease Associations by Incorporating Projections in Low-Dimensional Space and Local Topological
Ping Xuan1, Yan Zhang2, Tiangang Zhang3
1School of Computer Science and Technology, Heilongjiang University, Harbin 150080, China. xuanping@hlju.edu.cn.
Abstract:
Predicting the potential microRNA (miRNA) candidates associated with a disease helps in exploring the mechanisms of disease development. Most recent approaches have utilized heterogeneous information about miRNAs and diseases, including miRNA similarities, disease similarities, and miRNA-disease associations. However, these methods do not utilize the projections of miRNAs and diseases in a low-dimensional space. Thus, it is necessary to develop a method that can utilize the effective information in the low-dimensional space to predict potential disease-related miRNA candidates. We proposed a method based on non-negative matrix factorization, named DMAPred, to predict potential miRNA-disease associations. DMAPred exploits the similarities and associations of diseases and miRNAs, and it integrates local topological information of the miRNA network. The likelihood that a miRNA is associated with a disease also depends on their projections in low-dimensional space. Therefore, we project miRNAs and diseases into low-dimensional feature space to yield their low-dimensional and dense feature representations. Moreover, the sparse characteristic of miRNA-disease associations was introduced to make our predictive model more credible. DMAPred achieved superior performance for 15 well-characterized diseases with AUCs (area under the receiver operating characteristic curve) ranging from 0.860 to 0.973 and AUPRs (area under the precision-recall curve) ranging from 0.118 to 0.761. In addition, case studies on breast, prostatic, and lung neoplasms demonstrated the ability of DMAPred to discover potential disease-related miRNAs.
Insights
Predicting disease-related microRNAs (miRNAs) is crucial for understanding disease mechanisms. Our new method, DMAPred, uses low-dimensional projections and network information to accurately identify potential miRNA-disease associations.
Area of Science:
- Bioinformatics
- Genomics
- Computational Biology
Background:
- Identifying microRNA (miRNA) associations with diseases aids in understanding disease mechanisms.
- Current methods leverage miRNA/disease similarities and known associations but overlook low-dimensional projections.
- A need exists for methods incorporating low-dimensional feature representations for improved miRNA-disease prediction.
Purpose of the Study:
- To develop a novel computational method for predicting potential miRNA-disease associations.
- To integrate low-dimensional feature representations of miRNAs and diseases into a predictive model.
- To enhance the accuracy and credibility of miRNA-disease association predictions.
Main Methods:
- Proposed DMAPred, a method based on non-negative matrix factorization.
- Exploited miRNA/disease similarities, known associations, and miRNA network topology.
- Projected miRNAs and diseases into a low-dimensional feature space for dense representations.
- Incorporated the sparse nature of miRNA-disease associations.
Main Results:
- DMAPred demonstrated superior performance across 15 well-characterized diseases.
- Achieved high Area Under the Receiver Operating Characteristic Curve (AUC) values (0.860–0.973).
- Achieved significant Area Under the Precision-Recall Curve (AUPR) values (0.118–0.761).
- Case studies on breast, prostate, and lung neoplasms validated DMAPred's predictive capability.
Conclusions:
- DMAPred effectively predicts potential miRNA-disease associations by utilizing low-dimensional projections and network information.
- The method offers a credible and accurate approach for discovering novel disease-related miRNAs.
- This work contributes to advancing the understanding of miRNA roles in disease pathogenesis.
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