SVCA
SVCA quantifies contributions of tissue spatial structure and cell–cell interactions to gene and protein expression variance in single-cell multiplexed spatially resolved RNA and protein datasets, including Imaging Mass Cytometry.
Key Features:
- Quantification of Spatial Variation: Quantifies spatial variation in gene and protein expression attributable to tissue organization in spatial molecular datasets.
- Cell-Cell Interaction Analysis: Estimates and isolates the contribution of cell–cell interactions to expression variability at single-cell resolution.
- Variance Component Decomposition: Decomposes total expression variance into components attributable to tissue spatial structure, cell–cell interactions, and other sources.
- Interpretable Spatial Variance Signatures: Derives interpretable spatial variance signatures linking variance components to molecular patterns, demonstrated on breast cancer Imaging Mass Cytometry data.
- Identification of Gene Families: Identifies gene families associated with interaction-driven variance in high-dimensional imaging-derived RNA data.
Scientific Applications:
- Oncology (tumor heterogeneity): Dissects spatial organization and cellular heterogeneity in tumors, as exemplified by breast cancer Imaging Mass Cytometry analyses.
- Spatially resolved molecular profiling: Analyzes multiplexed spatially resolved RNA and protein expression at single-cell resolution to study cellular communication and microenvironmental effects.
Methodology:
Analyzes spatial molecular datasets by decomposing variance components to isolate contributions from tissue spatial structure and cell–cell interactions and derives interpretable spatial variance signatures.
Topics
Details
- License:
- Apache-2.0
- Programming Languages:
- C++, Python
- Added:
- 1/9/2020
- Last Updated:
- 11/24/2024
Operations
Publications
Arnol D, Schapiro D, Bodenmiller B, Saez-Rodriguez J, Stegle O. Modeling Cell-Cell Interactions from Spatial Molecular Data with Spatial Variance Component Analysis. Cell Reports. 2019;29(1):202-211.e6. doi:10.1016/j.celrep.2019.08.077. PMID:31577949. PMCID:PMC6899515.