Evidence map›Paper›PMID 38243704›Full record

ArticleBioinformatics (Oxford, England)2024

DESpace: spatially variable gene detection via differential expression testing of spatial clusters.

Peiying Cai, Mark D Robinson, Simone Tiberi

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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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

3 authors.

Peiying CaiDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich 8057, Switzerland.
Mark D RobinsonDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich 8057, Switzerland.ORCID 0000-0002-3048-5518
Simone TiberiDepartment of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Zurich 8057, Switzerland.ORCID 0000-0002-3054-9964

Funding

Swiss National Science Foundation 310030_175841
6 · The paper itself

Abstract

motivationSpatially resolved transcriptomics (SRT) enables scientists to investigate spatial context of mRNA abundance, including identifying spatially variable genes (SVGs), i.e. genes whose expression varies across the tissue. Although several methods have been proposed for this task, native SVG tools cannot jointly model biological replicates, or identify the key areas of the tissue affected by spatial variability.

resultsHere, we introduce DESpace, a framework, based on an original application of existing methods, to discover SVGs. In particular, our approach inputs all types of SRT data, summarizes spatial information via spatial clusters, and identifies spatially variable genes by performing differential gene expression testing between clusters. Furthermore, our framework can identify (and test) the main cluster of the tissue affected by spatial variability; this allows scientists to investigate spatial expression changes in specific areas of interest. Additionally, DESpace enables joint modeling of multiple samples (i.e. biological replicates); compared to inference based on individual samples, this approach increases statistical power, and targets SVGs with consistent spatial patterns across replicates. Overall, in our benchmarks, DESpace displays good true positive rates, controls for false positive and false discovery rates, and is computationally efficient. AVAILABILITY AND IMPLEMENTATION: DESpace is freely distributed as a Bioconductor R package at https://bioconductor.org/packages/DESpace.

Indexed as

Gene Expression ProfilingSoftwareTranscriptome

Identifiers

PMID38243704
PMCPMC10868334

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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.