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Updated: Apr 14, 2026

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Inferring data-specific micro-RNA function through the joint ranking of micro-RNA and pathways from matched micro-RNA
Ellis Patrick1, Michael Buckley2, Samuel Müller1
1School of Mathematics and Statistics, University of Sydney, Sydney, NSW 2006, Australia.
Motivation:
In practice, identifying and interpreting the functional impacts of the regulatory relationships between micro-RNA and messenger-RNA is non-trivial. The sheer scale of possible micro-RNA and messenger-RNA interactions can make the interpretation of results difficult.
Results:
We propose a supervised framework, pMim, built upon concepts of significance combination, for jointly ranking regulatory micro-RNA and their potential functional impacts with respect to a condition of interest. Here, pMim directly tests if a micro-RNA is differentially expressed and if its predicted targets, which lie in a common biological pathway, have changed in the opposite direction. We leverage the information within existing micro-RNA target and pathway databases to stabilize the estimation and annotation of micro-RNA regulation making our approach suitable for datasets with small sample sizes. In addition to outputting meaningful and interpretable results, we demonstrate in a variety of datasets that the micro-RNA identified by pMim, in comparison to simpler existing approaches, are also more concordant with what is described in the literature.
Availability And Implementation:
This framework is implemented as an R function, pMim, in the package sydSeq available from http://www.ellispatrick.com/r-packages.
Contact:
jean.yang@sydney.edu.au
Supplementary Information:
Supplementary data are available at Bioinformatics online.
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