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Modeling Cell-Cell Interactions from Spatial Molecular Data with Spatial Variance Component Analysis
DOI:10.1016/j.celrep.2019.08.077.png)
摘要
En 中文
Technological advances enable assaying multiplexed spatially resolvedRNAand protein expression profiling of individual cells, thereby capturing molecular variations in physiological contexts. While these methods are increasingly accessible, computational approaches for studying the interplay of the spatial structure of tissues and cell-cell heterogeneity are only beginning to emerge. Here, we present spatial variance component analysis (SVCA), a computational framework for the analysis of spatial molecular data. SVCA enables quantifying different dimensions of spatial variation and in particular quantifies the effect of cell-cell interactions on gene expression. In a breast cancer Imaging Mass Cytometry dataset, our model yields interpretable spatial variance signatures, which reveal cell-cell interactions as a major driver of protein expression heterogeneity. Applied to high-dimensional imaging-derived RNA data, SVCA identifies plausible gene families that are linked to cell-cell interactions. SVCA is available as a free software tool that can be widely applied to spatial data from different technologies.
Keyword:
GENE-EXPRESSION
NEUROTRANSMITTER TRANSPORTERS
SUBCELLULAR RESOLUTION
BREAST-CANCER
TISSUE
RNA
PHAGOCYTOSIS
DISCOVERY
RECEPTOR
CAMKII
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期刊
IF:
6.9
论文数:
1.7W
被引数:
10.2W
机构
引用论文
High-throughput single-cell gene-expression profiling with multiplexed error-robust fluorescence in situ hybridization具有多重错误的高通量单细胞基因表达谱-稳健的荧光原位杂交
High-throughput spatial mapping of single-cell RNA-seq data to tissue of origin单细胞rna-seq数据到原始组织的高通量空间映射
NATURE BIOTECHNOLOGY
IF41.7
Simultaneous Multiplexed Imaging of mRNA and Proteins with Subcellular Resolution in Breast Cancer Tissue Samples by Mass Cytometry
CELL SYSTEMS
IF7.7

