Evidence map›Paper›PMID 40662813›Full record

ArticleBioinformatics (Oxford, England)2025

Spatial transcriptomics deconvolution methods generalize well to spatial chromatin accessibility data.

Sarah Ouologuem, Laura D Martens, Anna C Schaar, Maiia Shulman, Julien Gagneur, Fabian J Theis

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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 2 papers.

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2citing papers in PubMed
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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Sarah OuologuemSchool of Computation, Information and Technology, Technical University of Munich, Munich, 80333, Germany.ORCID 0009-0005-3398-1700
Laura D MartensSchool of Computation, Information and Technology, Technical University of Munich, Munich, 80333, Germany.ORCID 0000-0001-6520-4029
Anna C SchaarSchool of Computation, Information and Technology, Technical University of Munich, Munich, 80333, Germany.ORCID 0000-0003-1063-005X
Maiia ShulmanComputational Health Center, Helmholtz Center Munich, Neuherberg, 85764, Germany.ORCID 0009-0006-6308-1997
Julien GagneurSchool of Computation, Information and Technology, Technical University of Munich, Munich, 80333, Germany.ORCID 0000-0002-8924-8365
Fabian J TheisSchool of Computation, Information and Technology, Technical University of Munich, Munich, 80333, Germany.ORCID 0000-0002-2419-1943

Funding

Deutsche ForschungsgemeinschaftEuropean Research CouncilEuropean Research Council 101054957German Network for Bioinformatics InfrastructureGerman Research Foundation 403584255German Research Foundation 461264291Helmholtz AssociationMunich School for Data ScienceNBI
6 · The paper itself

Abstract

motivationSpatially resolved chromatin accessibility profiling offers the potential to investigate gene regulatory processes within the spatial context of tissues. However, current methods typically work at spot resolution, aggregating measurements from multiple cells, thereby obscuring cell-type-specific spatial patterns of accessibility. Spot deconvolution methods have been developed and extensively benchmarked for spatial transcriptomics, yet no dedicated methods exist for spatial chromatin accessibility, and it is unclear if RNA-based approaches are applicable to that modality.

resultsHere, we demonstrate that these RNA-based approaches can be applied to spot-based chromatin accessibility data by a systematic evaluation of five top-performing spatial transcriptomics deconvolution methods. To assess performance, we developed a simulation framework that generates both transcriptomic and accessibility spot data from dissociated single-cell and targeted multiomic datasets, enabling direct comparisons across both data modalities. Our results show that Cell2location and RCTD, in contrast to other methods, exhibit robust performance on spatial chromatin accessibility data, achieving accuracy comparable to RNA-based deconvolution. Generally, we observed that RNA-based deconvolution exhibited slightly better performance compared to chromatin accessibility-based deconvolution, especially for resolving rare cell types, indicating room for future development of specialized methods. In conclusion, our findings demonstrate that existing deconvolution methods can be readily applied to chromatin accessibility-based spatial data. Our work provides a simulation framework and establishes a performance baseline to guide the development and evaluation of methods optimized for spatial epigenomics. AVAILABILITY AND IMPLEMENTATION: All methods, simulation frameworks, peak selection strategies, analysis notebooks and scripts are available at https://github.com/theislab/deconvATAC.

Indexed as

ChromatinComputational BiologyGene Expression ProfilingTranscriptomeHumansSingle-Cell AnalysisChromatin

Identifiers

PMID40662813
PMCPMC12261446

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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.