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Reference-free cell type deconvolution of multi-cellular pixel-resolution spatially resolved transcriptomics data

delete2022-04-29
delete71
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OA
AI
B
Brendan Miller
F
Feiyang Huang
L
Lyla Atta
A
Arpan Sahoo
J
Jean Fan *
DOI:10.1038/s41467-022-30033-zdelete
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Abstract

Abstract

En 中文
Recent technological advancements have enabled spatially resolved transcriptomic profiling but at multi-cellular pixel resolution, thereby hindering the identification of cell-type-specific spatial patterns and gene expression variation. To address this challenge, we develop STdeconvolve as a reference-free approach to deconvolve underlying cell types comprising such multi-cellular pixel resolution spatial transcriptomics (ST) datasets. Using simulated as well as real ST datasets from diverse spatial transcriptomics technologies comprising a variety of spatial resolutions such as Spatial Transcriptomics, 10X Visium, DBiT-seq, and Slide-seq, we show that STdeconvolve can effectively recover cell-type transcriptional profiles and their proportional representation within pixels without reliance on external single-cell transcriptomics references. STdeconvolve provides comparable performance to existing reference-based methods when suitable single-cell references are available, as well as potentially superior performance when suitable single-cell references are not available. STdeconvolve is available as an open-source R software package with the source code available at https://github.com/JEFworks-Lab/STdeconvolve.
Keywords:
GENOME-WIDE EXPRESSION
ADULT
MICROENVIRONMENT
HETEROGENEITY
PATHWAY
CANCER
SEQ
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Journal

Nature Communications cover
Nature Communications
IF:
15.7
Papers:
9.2W
Citations:
91.2W

Organization

J
Johns Hopkins University
Scholars:
10.2W
Papers: 8.8W
Citations: 13.0W