Evidence map›Paper›PMID 40981505›Full record

ArticleBioinformatics (Oxford, England)2025

DiSTect: a Bayesian model for disease-associated gene discovery and prediction in spatial transcriptomics.

Qicheng Zhao, Anji Deng, Qihuang Zhang

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. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Qicheng ZhaoDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec H3A 1G1, Canada.ORCID 0009-0004-2155-1781
Anji DengDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec H3A 1G1, Canada.
Qihuang ZhangDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec H3A 1G1, Canada.ORCID 0000-0003-1455-2159

Funding

Canadian Statistical Sciences Institute (CANSSI) QuebecFRQ-SantéNatural Sciences and Engineering Research Council of Canada (NSERC)Québec Research Scholar
6 · The paper itself

Abstract

motivationIdentifying disease-indicative genes is critical for deciphering disease mechanisms and has attracted significant interest in biomedical research. Spatial transcriptomics offers unprecedented insights for the detection of disease-associated genes by enabling within-tissue contrasts. However, this new technology poses challenges for conventional statistical models developed for RNA-sequencing, as these models often neglect the spatial corrleation of the disease status among tissue spots.

resultsIn this article, we propose DiSTect, a Bayesian shrinkage model to characterize the relationship between high-dimensional gene expressions and the disease status of each tissue spot, incorporating spatial correlation among these spots through autoregressive terms. Our model adopts a hierarchical structure to facilitate the analysis of multiple correlated samples and is further extended to accommodate the missing data within tissues. To ensure the model's applicability to datasets of varying sizes, we carry out two computational frameworks for Bayesian parameter estimation, tailored to both small and large sample scenarios. Simulation studies are conducted to evaluate the performance of the proposed model. The proposed model is applied to analyze the data arising from studies of HER2+ breast cancer and Alzheimer's disease. AVAILABILITY AND IMPLEMENTATION: The dataset and source code are available on GitHub (https://github.com/StaGill/DiSTect) and Zenodo (https://zenodo.org/records/17127211).

Indexed as

Gene Expression ProfilingSoftwareTranscriptomeAlgorithmsAlzheimer DiseaseBayes TheoremBreast NeoplasmsComputational BiologyFemaleHumans

Identifiers

PMID40981505
PMCPMC12502917

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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.