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Ranking of microRNA target prediction scores by Pareto front analysis
Sudhakar Sahoo1, Andreas A Albrecht
1Queen's University Belfast, Centre for Cancer Research and Cell Biology, Belfast BT9 7BL, UK.
Abstract:
Over the past ten years, a variety of microRNA target prediction methods has been developed, and many of the methods are constantly improved and adapted to recent insights into miRNA-mRNA interactions. In a typical scenario, different methods return different rankings of putative targets, even if the ranking is reduced to selected mRNAs that are related to a specific disease or cell type. For the experimental validation it is then difficult to decide in which order to process the predicted miRNA-mRNA bindings, since each validation is a laborious task and therefore only a limited number of mRNAs can be analysed. We propose a new ranking scheme that combines ranked predictions from several methods and - unlike standard thresholding methods - utilises the concept of Pareto fronts as defined in multi-objective optimisation. In the present study, we attempt a proof of concept by applying the new ranking scheme to hsa-miR-21, hsa-miR-125b, and hsa-miR-373 and prediction scores supplied by PITA and RNAhybrid. The scores are interpreted as a two-objective optimisation problem, and the elements of the Pareto front are ranked by the STarMir score with a subsequent re-calculation of the Pareto front after removal of the top-ranked mRNA from the basic set of prediction scores. The method is evaluated on validated targets of the three miRNA, and the ranking is compared to scores from DIANA-microT and TargetScan. We observed that the new ranking method performs well and consistent, and the first validated targets are elements of Pareto fronts at a relatively early stage of the recurrent procedure, which encourages further research towards a higher-dimensional analysis of Pareto fronts.
Insights
This study introduces a novel ranking scheme for microRNA (miRNA) targets, combining multiple prediction methods using Pareto fronts. The new method efficiently prioritizes experimentally validated miRNA targets, improving validation strategies.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Numerous microRNA (miRNA) target prediction methods exist, often yielding divergent results.
- Experimental validation of predicted miRNA-mRNA interactions is resource-intensive, necessitating efficient prioritization.
Purpose of the Study:
- To develop and validate a new ranking scheme for prioritizing miRNA targets by integrating predictions from multiple algorithms.
- To utilize Pareto front optimization for improved selection of miRNA-mRNA binding candidates for experimental validation.
Main Methods:
- A novel ranking scheme combining predictions from PITA and RNAhybrid was developed, employing Pareto front optimization.
- The scheme was applied to specific miRNAs (hsa-miR-21, hsa-miR-125b, hsa-miR-373) and validated using known targets.
- Performance was evaluated against DIANA-microT and TargetScan, using the STarMir score for ranking Pareto front elements.
Main Results:
- The proposed ranking method demonstrated consistent performance in identifying validated miRNA targets.
- Validated targets were found within Pareto fronts early in the recurrent ranking procedure.
- The approach offers a more effective strategy for prioritizing miRNA-mRNA interactions for experimental analysis.
Conclusions:
- The Pareto front-based ranking scheme provides a robust and efficient method for prioritizing miRNA targets.
- This approach facilitates experimental validation by highlighting high-confidence miRNA-mRNA interactions.
- Further research into higher-dimensional Pareto front analysis is warranted for enhanced miRNA target discovery.
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