regulAS: A Bioinformatics Tool for the Integrative Analysis of Alternative Splicing Regulome using RNA-Seq data
Sofya Lipnitskaya

TL;DR
regulAS is a comprehensive bioinformatics tool that automates and customizes the analysis of alternative splicing mechanisms using large-scale RNA-Seq data from cancer and healthy tissues, facilitating research in cancer biology.
Contribution
It introduces an extensible, user-friendly software package that integrates data retrieval, predictive modeling, and reporting for alternative splicing analysis in a reproducible workflow.
Findings
Automates large-scale RNA-Seq data analysis workflows.
Supports integration of multi-omics data for splicing studies.
Enhances reproducibility and customization in splicing research.
Abstract
The regulAS software package is a bioinformatics tool designed to support computational biology researchers in investigating regulatory mechanisms of splicing alterations through integrative analysis of large-scale RNA-Seq data from cancer and healthy human donors, characterized by TCGA and GTEx projects. This technical report provides a comprehensive overview of regulAS, focusing on its core functionality, basic modules, experiment configuration, further extensibility and customisation. The core functionality of regulAS enables the automation of computational experiments, efficient results storage and processing, and streamlined workflow management. Integrated basic modules extend regulAS with features such as RNA-Seq data retrieval from the public multi-omics UCSC Xena data repository, predictive modeling and feature ranking capabilities using the scikit-learn package, and flexible…
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Taxonomy
TopicsRNA Research and Splicing · RNA modifications and cancer · RNA and protein synthesis mechanisms
MethodsHydra
