Evidence map›Paper›PMID 42321172›Full record

ArticleNature communications2026

Scalable, fast and accurate differential gene expression testing from millions of cells of multiple patients.

Giovanni Santacatterina, Niccolò Tosato, Salvatore Milite, Katsiaryna Davydzenka, Edoardo Insaghi, Guido Sanguinetti, Stefano Cozzini, Leonardo Egidi, Giulio Caravagna

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Giovanni Santacatterina *Department of Mathematics, Informatics and Geosciences, University of Trieste, Trieste, Italy.ORCID http://orcid.org/0009-0003-8507-6521
Niccolò Tosato *Department of Mathematics, Informatics and Geosciences, University of Trieste, Trieste, Italy.
Salvatore MiliteCentre for Computational Biology, Human Technopole, Milan, Italy.ORCID http://orcid.org/0000-0002-0156-3636
Katsiaryna DavydzenkaTheoretical and Scientific Data Science Group, SISSA, Trieste, Italy.
Edoardo InsaghiDepartment of Mathematics, Informatics and Geosciences, University of Trieste, Trieste, Italy.
Guido SanguinettiTheoretical and Scientific Data Science Group, SISSA, Trieste, Italy.ORCID http://orcid.org/0000-0002-6663-8336
Stefano CozziniArea Science Park, Trieste, Italy.
Leonardo EgidiDepartment of Economics, Business, Mathematics and Statistics "Bruno de Finetti" (DEAMS), University of Trieste, Trieste, Italy. legidi@units.it.
Giulio CaravagnaDepartment of Mathematics, Informatics and Geosciences, University of Trieste, Trieste, Italy. gcaravagna@units.it.ORCID http://orcid.org/0000-0003-4240-3265

Funding

Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 24913Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 27631Associazione Italiana per la Ricerca sul Cancro (Italian Association for Cancer Research) 32107
6 · The paper itself

Abstract

Since the development of DNA microarrays and later RNA bulk sequencing, testing with statistically independent samples has been the standard method for detecting genes with different transcription patterns. Single-cell assays challenge these assumptions because individual cells are statistically dependent, and all proposed methodologies present mathematical limitations or computational bottlenecks that prevent a seamless integration of data from many cells and patients simultaneously. In this work, we solve this crucial limitation by introducing a Bayesian framework that retrieves the independence structure at the level of individual patients, separating differences across individuals from actual transcriptional differences. Leveraging multi-GPU and variational inference, our approach excels across different experimental designs and scales to analyse over 10 million cells. This framework enables single-cell differential expression analysis that can finally integrate datasets from large clinical cohorts, atlas projects, or drug-response screens with thousands of samples and millions of cells.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisAlgorithmsBayes TheoremHumansOligonucleotide Array Sequence AnalysisSingle-Cell Gene Expression Analysis

Identifiers

PMID42321172
PMCPMC13434233

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.