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

Nat Commun

Center for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD, 21211, United States.

Published: April 2022

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 .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9055051PMC
http://dx.doi.org/10.1038/s41467-022-30033-zDOI Listing

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