This repository contains the analysis files used in the manuscript to demonstrate the effectiveness of MIRit in integrative miRNA-mRNA analyses. For more information on how MIRit works, please refer to the original paper. The source code of MIRit is accessible on GitHub.
Dr. Jacopo Ronchi 1 (author and maintainer)
1School of Medicine and Surgery, University of Milano-Bicocca, Italy
The publication that details the implementation of MIRit and its usage is currently available on bioRxiv:
Ronchi J and Foti M. ‘MIRit: an integrative R framework for the identification of impaired miRNA-mRNA regulatory networks in complex diseases’. bioRxiv (2023). doi:10.1101/2023.11.24.568528
The performance of MIRit has been tested with three different datasets:
- A sample-matched experiment in which miRNA and mRNA expression were evaluated in patients with dilated cardiomyopathy using miRNA-Seq and RNA-Seq, respectively.
- A sample-matched experiment in which miRNA and mRNA expression were profiled in clear cell renal cell carcinoma (ccRCC) samples and normal adjacent renal tissue.
- A dataset without matched samples, in which miRNA expression was evaluated in postmortem BA9 tissue from a cohort of patients with Alzheimer's disease (AD) and gene expression was assessed using microarray technology in the same brain region, but in a different cohort of patients.
The datasets used in this study are publicly available on GEO under the accession numbers GSE243406, GSE16441, GSE63501, and GSE150696.
The R scripts used to generate the results presented in the manuscript can be found in the "Dilated Cardiomyopathy," "Clear Cell Renal Cell Carcinoma," and "Alzheimer's Disease" folders. R scripts used for data preprocessing are also included when necessary.