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Characterizing cell-type spatial relationships across length scales in spatially resolved omics data.
- Source :
- Nature Communications; 1/3/2025, Vol. 16 Issue 1, p1-14, 14p
- Publication Year :
- 2025
-
Abstract
- Spatially resolved omics (SRO) technologies enable the identification of cell types while preserving their organization within tissues. Application of such technologies offers the opportunity to delineate cell-type spatial relationships, particularly across different length scales, and enhance our understanding of tissue organization and function. To quantify such multi-scale cell-type spatial relationships, we present CRAWDAD, Cell-type Relationship Analysis Workflow Done Across Distances, as an open-source R package. To demonstrate the utility of such multi-scale characterization, recapitulate expected cell-type spatial relationships, and evaluate against other cell-type spatial analyses, we apply CRAWDAD to various simulated and real SRO datasets of diverse tissues assayed by diverse SRO technologies. We further demonstrate how such multi-scale characterization enabled by CRAWDAD can be used to compare cell-type spatial relationships across multiple samples. Finally, we apply CRAWDAD to SRO datasets of the human spleen to identify consistent as well as patient and sample-specific cell-type spatial relationships. In general, we anticipate such multi-scale analysis of SRO data enabled by CRAWDAD will provide useful quantitative metrics to facilitate the identification, characterization, and comparison of cell-type spatial relationships across axes of interest. Authors introduce CRAWDAD, an R package for quantifying cell-type spatial relationships across length scales in tissues using spatial omics data, enabling the identification of consistent as well as sample-specific celltype spatial relationships across multiple spatial omics datasets. [ABSTRACT FROM AUTHOR]
- Subjects :
- SPLEEN
DATA analysis
WORKFLOW
TISSUES
Subjects
Details
- Language :
- English
- ISSN :
- 20411723
- Volume :
- 16
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Nature Communications
- Publication Type :
- Academic Journal
- Accession number :
- 182074516
- Full Text :
- https://doi.org/10.1038/s41467-024-55700-1