Evidence map›Paper›PMID 40059456›Full record

ArticleSmall methods2025

Robust Spatial Cell-Type Deconvolution with Qualitative Reference for Spatial Transcriptomics.

Qishi Dong, Yi Yang, Ziye Luo, Haipeng Shen, Xingjie Shi, Jin Liu

Abstract read
In one paragraph

Article in Small methods, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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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

6 authors.

Qishi DongCollege of Big Data and Internet, Shenzhen Technology University, Shenzhen, 518118, China.ORCID 0009-0005-6994-598X
Yi YangThe Key Laboratory of Developmental Genes and Human Disease, School of Life Science and Technology, Southeast University, Nanjing, 210018, China.
Ziye LuoDepartment of Biometrics, Astrazeneca Global R&D (China) CO. Ltd., Shanghai, 200085, China.
Haipeng ShenFaculty of Business and Economics, Hong Kong University, Pokfulam, Hong Kong SAR, China.
Xingjie ShiKLATASDS-MOE, Academy of Statistics and Interdisciplinary Sciences, School of Statistics, East China Normal University, Shanghai, 200062, China.
Jin LiuSchool of Data Science, The Chinese University of Hong Kong-Shenzhen, Shenzhen, 518172, China.ORCID 0000-0002-5707-2078

Funding

Guangdong Provincial Key Laboratory of Mathematical Foundations for Artificial Intelligence 2023B1212010001HKU Education Consulting (Shenzhen) Co, LTD. SZRI2023-TBRF-03National Natural Science Foundation of China 12171229National Natural Science Foundation of China 12371283National Natural Science Foundation of China 92358303Natural Science Foundation of Shanghai Municipality 22ZR1420500Natural Science Foundation of Shanghai Municipality 23JS1400500Shenzhen Key Laboratory of Cross-Modal Cognitive Computing ZDSYS20230626091302006Shenzhen Stability Science Program 2024SC0010University Development Fund (Chinese University of Hong Kong (Shenzhen)) UDF01003033
6 · The paper itself

Abstract

Many spatially resolved transcriptomic technologies have been developed to provide gene expression profiles for spots that may contain heterogeneous mixtures of cells. To decompose cellular composition and expression levels, various deconvolution methods have been developed using single-cell RNA sequencing (scRNA-seq) data with known cell-type labels as a reference. However, in the absence of a reliable reference dataset or in the presence of heterogeneous batch effects, these methods may introduce bias. Here, a Qualitative-Reference-based Spatially-Informed Deconvolution method (QR-SIDE) is developed for multi-cellular spatial transcriptomic data. Uniquely, QR-SIDE provides a detailed map of spatial heterogeneity for individual marker genes and performs robust deconvolution by adaptively adjusting the contributions of each marker gene. Simultaneously, QR-SIDE unifies cell-type deconvolution with spatial clustering and incorporates spatial information via a Potts model to promote spatial continuity. The identified spatial domains represent a meaningful biological effect in potential tissue segments. Using simulated data and three real spatial transcriptomic datasets from the 10x Visium and ST platforms, QR-SIDE demonstrates improved accuracy and robustness in cell-type deconvolution and its superiority over established methods in recognizing and delineating spatial structures within a given context. These results can facilitate a range of downstream analyses and provide a refined understanding of cellular heterogeneity.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisTranscriptomeAlgorithmsAnimalsCluster AnalysisHumansMiceSequence Analysis, RNAcell‐type deconvolutionmixture Poisson regression modelPoisson factor modelspatial transcriptomics

Identifiers

PMID40059456
PMCPMC12103236

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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.