Evidence map›Paper›PMID 39865128›Full record

ArticleNature communications2025

Statistical identification of cell type-specific spatially variable genes in spatial transcriptomics.

Lulu Shang, Peijun Wu, Xiang Zhou

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. S3RL: Enhancing Spatial Single-Cell Transcriptomics With Separable Representation Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  9. Article
  10. A complete spatial map of mouse retinal ganglion cells reveals density and gene expression specializations.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. A unified framework for identification of cell-type-specific spatially variable genes in spatial transcriptomic studies.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

3 authors.

Lulu Shang *Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-2480-3065
Peijun Wu *Department of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA. xzhousph@umich.edu.ORCID http://orcid.org/0000-0002-4331-7599

Funding

Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing StudiesR01HG009124 · NHGRI · YALE UNIVERSITY · PI Xiang Zhou · 2017 to 2026
$3.0M
New directions in single cell genomics method developmentR01GM126553 · NIGMS · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2017 to 2026
$2.9M
Develop new bioinformatics infrastructures and computational tools for epitranscriptomics dataR01HG012927 · NHGRI · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2023 to 2026
$1.6M
Developing new computational tools for spatial transcriptomics dataR01HG011883 · NHGRI · UNIVERSITY OF CHICAGO · PI CHEN, MENGJIE, ZHOU, XIANG · 2021 to 2024
$1.5M
DMS/NIGMS 2: Advanced Statistical Methods for Spatially Resolved Transcriptomics StudiesR01GM144960 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, XIANG · 2021 to 2024
$1.3M
NHGRI NIH HHS R01 HG009124NHGRI NIH HHS R01 HG011883NHGRI NIH HHS R01 HG012927NIGMS NIH HHS R01 GM126553NIGMS NIH HHS R01 GM144960U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG009124U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) R01HG011883U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM126553U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM144960
6 · The paper itself

Abstract

An essential task in spatial transcriptomics is identifying spatially variable genes (SVGs). Here, we present Celina, a statistical method for systematically detecting cell type-specific SVGs (ct-SVGs)-a subset of SVGs exhibiting distinct spatial expression patterns within specific cell types. Celina utilizes a spatially varying coefficient model to accurately capture each gene's spatial expression pattern in relation to the distribution of cell types across tissue locations, ensuring effective type I error control and high power. Celina proves powerful compared to existing methods in single-cell resolution spatial transcriptomics and stands as the only effective solution for spot-resolution spatial transcriptomics. Applied to five real datasets, Celina uncovers ct-SVGs associated with tumor progression and patient survival in lung cancer, identifies metagenes with unique spatial patterns linked to cell proliferation and immune response in kidney cancer, and detects genes preferentially expressed near amyloid-β plaques in an Alzheimer's model.

Indexed as

Gene Expression ProfilingTranscriptomeAlzheimer DiseaseHumansKidney NeoplasmsLung NeoplasmsPlaque, AmyloidSingle-Cell Analysis

Identifiers

PMID39865128
PMCPMC11770176

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.