Evidence map›Paper›PMID 41053561›Full record

ArticleBMC genomics2025

Differential detection workflows for multi-sample single-cell RNA-seq data.

Jeroen Gilis, Laura Perin, Milan Malfait, Helena L Crowell, Koen Van den Berge, Alemu Takele Assefa, Bie Verbist, Davide Risso, Lieven Clement

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. bioRxiv : the preprint server for biology · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Jeroen Gilis *Department of Mathematics, Computer science and Statistics, Ghent University, Krijgslaan 281, Ghent, 9000, Belgium.
Laura Perin *Department of Statistical Sciences, University of Padova, Via C. Battisti 241, Padova, 35121, Italy.
Milan MalfaitDepartment of Mathematics, Computer science and Statistics, Ghent University, Krijgslaan 281, Ghent, 9000, Belgium.
Helena L CrowellCentro Nacional de Análisis Genómico, Carrer de Baldiri Reixac 4, torre i, Barcelona, 08028, Spain.
Koen Van den BergeStatistics and Decision Sciences, Johnson and Johnson Innovative Medicine, Turnhoutseweg 30, Beerse, 2340, Belgium.
Alemu Takele AssefaStatistics and Decision Sciences, Johnson and Johnson Innovative Medicine, Turnhoutseweg 30, Beerse, 2340, Belgium.
Bie VerbistStatistics and Decision Sciences, Johnson and Johnson Innovative Medicine, Turnhoutseweg 30, Beerse, 2340, Belgium.
Davide RissoDepartment of Statistical Sciences, University of Padova, Via C. Battisti 241, Padova, 35121, Italy.
Lieven ClementDepartment of Mathematics, Computer science and Statistics, Ghent University, Krijgslaan 281, Ghent, 9000, Belgium. lieven.clement@ugent.be.

Funding

Cancer Genomics: Integrative and Scalable Solutions in R/BioconductorU24CA289073 · NCI · GRADUATE SCHOOL OF PUBLIC HEALTH AND HEALTH POLICY · PI Sean Davis, Levi Waldron · 2024 to 2026
$3.2M
Chan Zuckerberg Initiative DAF CZF2019-002443Fonds Wetenschappelijk Onderzoek G062219NMUR PNRR CN00000013 CN1NCI NIH HHS U24 CA289073NIH HHS U24CA289073Swiss National Science Foundation 222136
6 · The paper itself

Abstract

In single-cell transcriptomics, differential expression (DE) tools compare average expression between cell types or conditions. However, scRNA-seq technologies hold the promise to infer differences in other aspects of the expression distribution. We therefore developed workflows for differential detection (DD) to infer differences in the average fraction of cells in which expression is detected. After benchmarking eight DD strategies, we present a unified workflow for jointly assessing DE and DD. Through simulations and two case studies, we demonstrate that our joint analyses provide complementary information, both in terms of the individual genes they report and in their functional interpretation.

Indexed as

Gene Expression ProfilingRNA-SeqSequence Analysis, RNASingle-Cell AnalysisComputational BiologyHumansSingle-Cell Gene Expression AnalysisTranscriptomeWorkflowbenchmarkingPresence/Absencepseudobulk aggregationscRNAseq data analysis

Identifiers

PMID41053561
PMCPMC12502395

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.