Evidence map›Paper›PMID 40511994›Full record

ArticleBioinformatics (Oxford, England)2025

Gene spatial integration: enhancing spatial transcriptomics analysis via deep learning and batch effect mitigation.

Rian Pratama, Jason Hilton, J Michael Cherry, Giltae Song

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 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. Review
  2. Review
  3. Computer Vision Methods for Spatial Transcriptomics: A Survey.bioRxiv : the preprint server for biology · 2025
    Article
  4. Review
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

4 authors.

Rian PratamaSchool of Computer Science and Engineering, Pusan National University, Busan 46241, South Korea.ORCID 0009-0000-8142-7126
Jason HiltonDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA 94304, United States.
J Michael CherryDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA 94304, United States.
Giltae SongSchool of Computer Science and Engineering, Pusan National University, Busan 46241, South Korea.ORCID 0000-0001-8796-4678

Funding

Artificial Intelligence Convergence Innovation Human Resources IITP-2025-RS-2023-00254177]Institute of Information & communications Technology Planning & Evaluation
6 · The paper itself

Abstract

motivationSpatial transcriptomics (ST) is a groundbreaking technique for studying the correlation between cellular organization within a tissue and its physiological and pathological properties. Every facet of spatial information, including cell/spot proximity, distribution, and dimensionality, is significant. Most methods lean heavily on proximity for ST analysis, each resulting in useful insights but still leaving other aspects untapped. In addition, samples procured at different times, by different donors, and by different technologies introduce a batch effects problem that hinders the statistical approach employed by most analysis tools. Addressing these challenges, we have developed a deep learning method for analyzing integrated multiple ST data, focusing on the distribution aspect. Furthermore, our method aims to leverage single-cell analysis tools.

resultsOur study introduces Gene Spatial Integration (GSI), a data integration pipeline utilizing a representation learning approach to extract the spatial distribution of genes into the same feature space as gene expression features. We employ an autoencoder network to extract spatial embedding, facilitating the projection of spatial features into gene expression feature space. Our approach allows for seamless integration of multiple samples with minimum detriment, increasing the performance of the ST data analysis tool. We show the application of our method on the human dorsolateral prefrontal cortex dataset. Our method consistently improves the performance of the clustering of Seurat tools, with the most significant increase observed in sample 151673, almost doubling the ARI score from 0.225 to 0.405. We also combine our pipeline with the clustering of GraphST, achieving a significantly higher ARI score in sample 151672 from 0.614 to 0.795. This result reveals the potential of gene distribution spatial aspect, also emphasizes the impact of integration and batch effect removal in developing a refined analysis in understanding tissue characteristics. AVAILABILITY AND IMPLEMENTATION: Implementation of GSI is accessible at https://github.com/Riandanis/Spatial_Integration_GSI.

Indexed as

Deep LearningGene Expression ProfilingTranscriptomeComputational BiologyHumansSingle-Cell Analysis

Identifiers

PMID40511994
PMCPMC12208067

What OpenQuestion holds

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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.