Evidence map›Paper›PMID 38887902›Full record

ArticleBiostatistics (Oxford, England)2024

DifferentialRegulation: a Bayesian hierarchical approach to identify differentially regulated genes.

Simone Tiberi, Joël Meili, Peiying Cai, Charlotte Soneson, Dongze He, Hirak Sarkar, Alejandra Avalos-Pacheco, Rob Patro, Mark D Robinson

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. diffGEK: differential gene expression kinetics.Bioinformatics (Oxford, England) · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Simone TiberiDepartment of Statistical Sciences, University of Bologna, Via delle Belle Arti 41, Bologna, 40126, Italy.ORCID 0000-0002-3054-9964
Joël MeiliDepartment of Molecular Life Sciences and SIB Swiss Institute of Bioinformatics, University of Zurich, Winterthurerstrasse 190, Zurich, 8057, Switzerland.ORCID 0009-0009-9428-6217
Peiying CaiDepartment of Molecular Life Sciences and SIB Swiss Institute of Bioinformatics, University of Zurich, Winterthurerstrasse 190, Zurich, 8057, Switzerland.
Charlotte SonesonComputational Biology Platform, Friedrich Miescher Institute for Biomedical Research and SIB Swiss Institute of Bioinformatics, Fabrikstrasse 24, Basel, 4056, Switzerland.
Dongze HeDepartment of Cell Biology and Molecular Genetics, University of Maryland, 4062 Campus Drive, College Park, MD 20742, United States.ORCID 0000-0001-8259-7434
Hirak SarkarDepartment of Computer Science, Princeton University, 35 Olden St, Princeton, NJ 08540, United States.
Alejandra Avalos-PachecoResearch Unit of Applied Statistics, TU Wien, Wiedner Hauptstrabe 8-10/105, Wien 1040, Austria.ORCID 0000-0001-5314-1681
Rob PatroCenter for Bioinformatics and Computational Biology, University of Maryland, 8125 Paint Branch Dr, College Park, MD 20742, United States.ORCID 0000-0001-8463-1675
Mark D RobinsonDepartment of Molecular Life Sciences and SIB Swiss Institute of Bioinformatics, University of Zurich, Winterthurerstrasse 190, Zurich, 8057, Switzerland.ORCID 0000-0002-3048-5518

Funding

Swiss National Science Foundation 310030_175841University Research Priority Program Evolution in Action at the University of Zurich
6 · The paper itself

Abstract

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.

Indexed as

Bayes TheoremGene Expression ProfilingGene Expression RegulationHumansModels, StatisticalRNA, MessengerRNA SplicingRNA, MessengerBayesian hierarchical modelBayesian inferencebioinformaticslatent variablesRNA-sequencing datastatistical software tooltranscriptomics

Identifiers

PMID38887902
PMCPMC11639160

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.