DEEPsc

DEEPsc imputes spatial coordinates onto scRNA-seq datasets using a spatial reference atlas to restore tissue spatial context for analyses of cell fate decisions and microenvironmental interactions.


Key Features:

  • System-Adaptive Deep Learning Approach: A deep learning framework that adapts to the specific characteristics of input data to map spatial coordinates from a reference atlas onto scRNA-seq datasets.
  • Comprehensive Evaluation Metrics: A set of metrics designed to evaluate accuracy, precision, and robustness of spatial mapping methods.
  • Comparative Performance Across Biological Systems: Comparative analyses across four different biological systems showing comparable accuracy to existing methods with an improved balance between precision and robustness.
  • Data-Adaptive Integration with Spatial Imaging: Connects scRNA-seq datasets with spatial imaging data to enable spatially informed exploration of cell fate decisions.

Scientific Applications:

  • Cell Fate Analysis: Restores spatial context in scRNA-seq data to analyze cell fate decisions within native tissue architecture.
  • Developmental Biology: Enables study of spatial arrangements and their influence on cell differentiation during development.
  • Oncology: Supports examination of tumor microenvironment and spatial cellular interactions in cancer research.
  • Tissue Engineering: Assists assessment of spatial organization and cellular context in engineered tissues.

Methodology:

Employs a system-adaptive deep learning framework to impute spatial coordinates from a spatial reference atlas onto scRNA-seq datasets, evaluates mapping using metrics for accuracy, precision, and robustness, performs comparative analyses across four biological systems, and integrates scRNA-seq with spatial imaging data.

Topics

Details

Programming Languages:
MATLAB, Java
Added:
9/8/2021
Last Updated:
9/13/2021

Operations

Publications

Maseda F, Cang Z, Nie Q. DEEPsc: A Deep Learning-Based Map Connecting Single-Cell Transcriptomics and Spatial Imaging Data. Frontiers in Genetics. 2021;12. doi:10.3389/fgene.2021.636743. PMID:33833776. PMCID:PMC8021700.

PMID: 33833776
PMCID: PMC8021700
Funding: - National Institutes of Health: P30AR075047, U01AR073159 - Simons Foundation: 594598, QN - National Science Foundation: DMS1763272, MCB2028424

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