Evidence map›Paper›PMID 42635194›Full record

ArticleBioinformatics (Oxford, England)2026

DESpace2: detection of differential spatial patterns in spatial omics data.

Peiying Cai, Mark D Robinson, Simone Tiberi

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Peiying CaiDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID 0009-0001-9229-2244
Mark D RobinsonDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-3048-5518
Simone TiberiDepartment of Statistical Sciences, University of Bologna, Bologna, Italy.ORCID 0000-0002-3054-9964

Funding

National Science Foundation 310030_204869University Research Priority Program Evolution in Action at the University of Zurich
6 · The paper itself

Abstract

motivationSpatially resolved transcriptomics (SRT) enables the investigation of mRNA expression in a spatial context. While several SRT analysis frameworks have been developed, the vast majority of them focus on analyzing individual samples, and do not allow for comparisons of spatial gene expression patterns across experimental conditions, such as healthy vs. diseased states.

resultsHere, we present an approach to identify so-called differential spatial patterns (DSP), i.e. genes that exhibit changes in spatial expression between groups of samples across conditions. Our framework processes diverse SRT data types and detects DSP by performing differential gene expression testing across conditions. Notably, this comparison is not currently available in any other spatial omics method. In addition to detecting DSP across conditions, our framework includes two key features. First, it can identify tissue regions where expression changes across conditions. Second, it can detect spatial gene expression pattern changes across more than two experimental conditions, with flexible models. With ad hoc simulations, we demonstrate that our approach has good true positive rates and well-calibrated false discovery rates. Applied to experimental data, our method identifies biologically relevant DSP genes while maintaining computational efficiency. AVAILABILITY: Our framework has been implemented within DESpace Bioconductor R package (from version 2.0.0).

Indexed as

Computational BiologyGene Expression ProfilingSoftwareTranscriptomeAlgorithmsSpatial Transcriptomics

Identifiers

PMID42635194
PMCPMC13501297

What Socratic holds

Textmetadata
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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 Socratic graph.