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Updated review of advances in microRNAs and complex diseases: towards systematic evaluation of computational models
Li Huang1,2, Li Zhang3, Xing Chen3,4
1Academy of Arts and Design, Tsinghua University, Beijing, 10084, China.
Abstract:
Currently, there exist no generally accepted strategies of evaluating computational models for microRNA-disease associations (MDAs). Though K-fold cross validations and case studies seem to be must-have procedures, the value of K, the evaluation metrics, and the choice of query diseases as well as the inclusion of other procedures (such as parameter sensitivity tests, ablation studies and computational cost reports) are all determined on a case-by-case basis and depending on the researchers' choices. In the current review, we include a comprehensive analysis on how 29 state-of-the-art models for predicting MDAs were evaluated. Based on the analytical results, we recommend a feasible evaluation workflow that would suit any future model to facilitate fair and systematic assessment of predictive performance.
Insights
No standard methods exist for evaluating microRNA-disease association (MDA) prediction models. This review analyzes 29 models and proposes a standardized workflow for consistent performance assessment.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Established evaluation strategies for microRNA-disease association (MDA) prediction models are lacking.
- Current model evaluation relies on researcher-dependent choices for K-fold cross-validation parameters, metrics, and study designs.
- Inconsistency in evaluation hinders fair comparison and systematic assessment of predictive performance.
Approach:
- A comprehensive analysis of evaluation methodologies employed by 29 state-of-the-art MDA prediction models was conducted.
- The study systematically reviewed practices including K-fold cross-validation, case studies, parameter sensitivity tests, and ablation studies.
- The analysis focused on identifying commonalities, variations, and potential areas for standardization.
Key Points:
- Evaluation metrics and procedures for MDA models vary significantly across studies.
- Parameters like K in cross-validation, query disease selection, and additional tests are not standardized.
- A lack of standardized evaluation limits the reproducibility and comparability of MDA prediction models.
Conclusions:
- A need exists for a universally accepted framework for evaluating computational MDA models.
- The proposed evaluation workflow aims to provide a systematic and fair method for assessing predictive performance.
- Implementing this workflow will enhance the reliability and comparability of future MDA prediction models.
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