Evidence map›Paper›PMID 40948400›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Multiscale Cell-Cell Interactive Spatial Transcriptomics Analysis.

Sean Cottrell, Guo-Wei Wei

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Multiscale Cell-Cell Interactive Spatial Transcriptomics Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Sean CottrellDepartment of Mathematics, Michigan State University, East Lansing, MI, 48824, USA.
Guo-Wei WeiDepartment of Mathematics, Michigan State University, East Lansing, MI, 48824, USA.ORCID https://orcid.org/0000-0002-5781-2937

Funding

AI-based platform for predicting emerging vaccine-escape variants and designing mutation-proof antibodiesR01AI164266 · NIAID · UNIVERSITY OF GEORGIA · PI Guowei Wei, YONG-HUI ZHENG · 2022 to 2026
$2.7M
Discovery-Driven Mathematics and Artificial Intelligence for Biosciences and Drug DiscoveryR35GM148196 · NIGMS · UNIVERSITY OF GEORGIA · PI Guowei Wei · 2023 to 2026
$1.5M
Synergistic integration of topology and machine learning for the predictions of protein-ligand binding affinities and mutation impactsR01GM126189 · NIGMS · MICHIGAN STATE UNIVERSITY · PI WEI, GUOWEI · 2018 to 2021
$1.4M
Bristol-Myers Squibb 65109Michigan State UniversityNational Science Foundation DMS2052983National Science Foundation IIS-190047NIAID NIH HHS R01 AI164266NIGMS NIH HHS R01 GM126189NIGMS NIH HHS R35 GM148196NIH Blueprint for Neuroscience Research 01GM126189NIH Blueprint for Neuroscience Research R01AI164266NIH Blueprint for Neuroscience Research R35GM148196
6 · The paper itself

Abstract

Spatial transcriptomics data analysis integrates gene expression profiles with their corresponding spatial locations to identify spatial domains, infer cell-type dynamics, and detect gene expression patterns within tissues. However, the current spatial transcriptomics analysis neglects the multiscale cell-cell interactions that are crucial in biology. To fill this gap, multiscale cell-cell interactive spatial transcriptomics (MCIST) analysis is proposed. MCIST combines the advantages of an ensemble of multiscale topological representations of cell-cell interactions in the gene expression space with those of cutting edge spatial deep learning techniques. MCIST is validated by a comparison of 14 cutting-edge methods on a huge collection of 37 benchmark spatial transcriptomics datasets. It is demonstrated that MCIST yields superior performance in spatial domain detection. It achieves the best clustering score on 23/37 datasets and is among the top three methods on 33/37 datasets, while the second best method scored only 6/37 and 17/37 on these measures, respectively. In terms of overall performance with respect to a quantitative metric, MCIST offers more than an 11% improvement to the previous state-of-the-art in spatial domain detection. In addition, MCIST offers multiscale insights with respect to trajectory inference, differentially expressed gene detection, and signaling pathway enrichment analysis. This MCIST sheds valuable light on the multiscale perspective in spatial transcriptomics.

Indexed as

Cell CommunicationComputational BiologyGene Expression ProfilingTranscriptomeDeep LearningHumansdeep learningmultiscale cell–cell interactionspersistent Laplacianspatial transcriptomics

Identifiers

PMID40948400
PMCPMC12667549

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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 OpenQuestion graph.