Evidence map›Paper›PMID 42045691›Full record

ArticleNature genetics2026

Interpretable, flexible and spatially aware integration of multiple spatial transcriptomics datasets from diverse sources.

Jia Zhao, Xiangyu Zhang, Gefei Wang, Yingxin Lin, Tianyu Liu, Rui B Chang, Hongyu Zhao

Abstract read
In one paragraph

Article in Nature genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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
  5. POPARI: Modeling multisample variation in spatial transcriptomics.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Jia ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-9107-8852
Xiangyu ZhangDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.
Gefei WangDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-5627-9918
Yingxin LinDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-4299-7326
Tianyu LiuDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-9412-6573
Rui B ChangDepartment of Neuroscience, School of Medicine, Yale University, New Haven, CT, USA.ORCID http://orcid.org/0000-0001-6953-2943
Hongyu ZhaoDepartment of Biostatistics, School of Public Health, Yale University, New Haven, CT, USA. hongyu.zhao@yale.edu.ORCID http://orcid.org/0000-0003-1195-9607

Funding

Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Kurt A Schalper · 2015 to 2026
$31.1M
Laboratory, Data Analysis, and Coordinating Center (LDACC) for the Developmental Human Genotype-Tissue Expression ProjectU24HG012108 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, HUTTNER, ANITA JULIANE · 2021 to 2025
$8.7M
Understanding the molecular and functional architecture of diverse body-brain pathwaysR01AT012041 · NCCIH · YALE UNIVERSITY · PI CHANG, RUI · 2022 to 2025
$3.0M
Computational and Statistical Methods to determine variant effect across cell types and development stagesU01HG013840 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, ZHAO, HONGYU · 2024 to 2024
$1.9M
NCCIH NIH HHS R01 AT012041NCI NIH HHS P50 CA196530NHGRI NIH HHS U01 HG013840NHGRI NIH HHS U24 HG012108Paul G. Allen Family Foundation The Allen Discovery Center program
6 · The paper itself

Abstract

Recent advances in spatial transcriptomics (ST) have generated an expanding collection of heterogeneous datasets, offering unprecedented opportunities to investigate tissue organizations and functions. However, effective interpretation and integration of data originating from diverse sources and conditions remain a major challenge. We present INSPIRE, a deep-learning method for interpretable, integrative analysis of multiple ST datasets. INSPIRE adopts an adversarial learning strategy with graph neural networks to achieve spatially informed and adaptive data integration. By incorporating non-negative matrix factorization, INSPIRE identifies interpretable spatial factors and associated gene programs that characterize tissue architecture, cell-type organization and biological processes. Across a broad range of applications, INSPIRE demonstrates superior performance in resolving fine-grained biological signals, integrating complementary strengths across technologies, capturing condition-specific variation, uncovering tumor microenvironment heterogeneity, elucidating developmental dynamics and facilitating three-dimensional tissue reconstruction. INSPIRE also scales to extremely large datasets, as demonstrated by applications to Xenium-profiled human breast cancer and Stereo-seq mouse organogenesis datasets.

Indexed as

Spatial TranscriptomicsTranscriptomeAnimalsBreast NeoplasmsDeep LearningFemaleGene Expression ProfilingGraph Neural NetworksHumansMiceTumor Microenvironment

Identifiers

PMID42045691
PMCPMC13175893

What OpenQuestion holds

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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.