Evidence map›Paper›PMID 41916308›Full record

ArticleCell reports methods2026

Multiscale domain identification for spatial transcriptomics via persistent homology.

Perry Beamer, Zixuan Cang

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Perry BeamerDepartment of Mathematics, North Carolina State University, Raleigh, NC, USA.
Zixuan CangDepartment of Mathematics, North Carolina State University, Raleigh, NC, USA; Center for Research in Scientific Computation, North Carolina State University, Raleigh, NC, USA. Electronic address: zcang@ncsu.edu.

Funding

Development of tools for analyzing cell-cell communication using spatial transcriptomic dataR01GM152494 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI Zixuan Cang, Qing Nie · 2024 to 2026
$1.0M
NIGMS NIH HHS R01 GM152494
6 · The paper itself

Abstract

Spatial transcriptomics (ST) measures gene expression at a set of spatial locations in a tissue. Communities of nearby cells that express similar genes form spatial domains. Specialized clustering algorithms have been developed to identify spatial domains. These methods often locate spatial domains at a single morphological scale, and interactions across multiple scales are often overlooked. For example, large domains often contain smaller substructures and heterogeneous regions may lie between homogeneous domains. Topological data analysis (TDA) is an emerging mathematical toolkit that studies the underlying features of data at various geometric scales, especially useful for analyzing biological datasets with multiscale characteristics. Using TDA, we develop persistent homology for domains at multiple scales (PHD-MS) to locate tissue structures that persist across morphological scales. We apply PHD-MS to highlight multiscale spatial domains across tissue types and ST technologies. We compare PHD-MS domains against expert-annotated ground truth, where PHD-MS outperforms traditional clustering approaches.

Indexed as

Spatial TranscriptomicsTranscriptomeAlgorithmsAnimalsCluster AnalysisClustering AlgorithmsComputational BiologyGene Expression ProfilingHumansCP: computational biologyCP: systems biologymultiscale domainsspatial transcriptomicstopological data analysis

Identifiers

PMID41916308
PMCPMC13198003

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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.