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.