DifferentialRegulation: a Bayesian hierarchical approach to identify differentially regulated genes

Author:

Tiberi Simone12ORCID,Meili Joël2ORCID,Cai Peiying2,Soneson Charlotte3,He Dongze45ORCID,Sarkar Hirak6,Avalos-Pacheco Alejandra78ORCID,Patro Rob59ORCID,Robinson Mark D2ORCID

Affiliation:

1. Department of Statistical Sciences, University of Bologna , Via delle Belle Arti 41, Bologna, 40126, Italy

2. Department of Molecular Life Sciences and SIB Swiss Institute of Bioinformatics, University of Zurich , Winterthurerstrasse 190, Zurich, 8057, Switzerland

3. Computational Biology Platform, Friedrich Miescher Institute for Biomedical Research and SIB Swiss Institute of Bioinformatics , Fabrikstrasse 24, Basel, 4056, Switzerland

4. Department of Cell Biology and Molecular Genetics, University of Maryland , 4062 Campus Drive, College Park, MD 20742, United States

5. Center for Bioinformatics and Computational Biology, University of Maryland, 8125 Paint Branch Dr, College Park, MD 20742, United States

6. Department of Computer Science, Princeton University , 35 Olden St, Princeton, NJ 08540, United States

7. Research Unit of Applied Statistics , TU Wien, Wiedner Hauptstrabe 8-10/105, Wien 1040, Austria

8. Harvard-MIT Center for Regulatory Science, Harvard Medical School , 200 Longwood Avenue, Boston, MA 02115200 Longwood Avenue, Boston, MA 02115, United States

9. Department of Computer Science, University of Maryland, 8125 Paint Branch Dr, College Park, MD 20742, United States

Abstract

Summary Although transcriptomics data is typically used to analyze mature spliced mRNA, recent attention has focused on jointly investigating spliced and unspliced (or precursor-) mRNA, which can be used to study gene regulation and changes in gene expression production. Nonetheless, most methods for spliced/unspliced inference (such as RNA velocity tools) focus on individual samples, and rarely allow comparisons between groups of samples (e.g. healthy vs. diseased). Furthermore, this kind of inference is challenging, because spliced and unspliced mRNA abundance is characterized by a high degree of quantification uncertainty, due to the prevalence of multi-mapping reads, ie reads compatible with multiple transcripts (or genes), and/or with both their spliced and unspliced versions. Here, we present DifferentialRegulation, a Bayesian hierarchical method to discover changes between experimental conditions with respect to the relative abundance of unspliced mRNA (over the total mRNA). We model the quantification uncertainty via a latent variable approach, where reads are allocated to their gene/transcript of origin, and to the respective splice version. We designed several benchmarks where our approach shows good performance, in terms of sensitivity and error control, vs. state-of-the-art competitors. Importantly, our tool is flexible, and works with both bulk and single-cell RNA-sequencing data. DifferentialRegulation is distributed as a Bioconductor R package.

Funder

Swiss National Science Foundation

University Research Priority Program Evolution in Action at the University of Zurich

Publisher

Oxford University Press (OUP)

Reference39 articles.

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