CPPLS_MLP

CPPLS_MLP constructs cell-cell communication networks and identifies highly variable genes (HVGs) associated with intercellular communication from scRNA-seq and spatial transcriptomics data.


Key Features:

  • Integration of scRNA-seq and spatial transcriptomics: Combines scRNA-seq and spatial transcriptomics datasets to capture spatial and single-cell expression patterns relevant to cell-cell communication.
  • Identification of Highly Variable Genes (HVGs): Identifies HVGs that are closely linked to intercellular communication and cell-type-specific expression variability.
  • Multiple Input Multiple Output (MIMO) analysis: Applies a MIMO framework to assess how neighboring cell types and intercellular signals affect differential expression of HVGs.
  • Network construction via ligand-receptor interactions: Constructs cell-cell communication networks by analyzing ligand-receptor interactions at multiple spatial and cellular scales.
  • Performance versus CCPLS: Demonstrates enhanced accuracy in network construction and identification of cell-type-specific HVGs compared with CCPLS.

Scientific Applications:

  • Immunology: Maps intercellular signaling and HVGs to investigate immune cell interactions and immune processes.
  • Developmental biology: Dissects cell–cell communication and HVG dynamics relevant to developmental processes and organismal homeostasis.

Methodology:

Uses scRNA-seq and spatial transcriptomics for data acquisition; constructs cell-cell communication networks by analyzing ligand-receptor interactions at multiple scales; identifies HVGs associated with intercellular communication using algorithmic approaches; and applies a Multiple Input Multiple Output (MIMO) framework to analyze effects of neighboring cell types on HVG differential expression.

Topics

Details

Cost:
Free of charge
Tool Type:
library
Programming Languages:
R, Python
Added:
7/18/2024
Last Updated:
11/24/2024

Operations

Publications

Zhang T, Wu Z, Li L, Ren J, Zhang Z, Wang G. CPPLS-MLP: a method for constructing cell–cell communication networks and identifying related highly variable genes based on single-cell sequencing and spatial transcriptomics data. Briefings in Bioinformatics. 2024;25(3). doi:10.1093/bib/bbae198. PMID:38678387. PMCID:PMC11056015.

PMID: 38678387
Funding: - National Key Research and Development Program of China: 2022YFF1202100 - National Natural Science Foundation of China: 62072095, 62172087 - National Science Foundation for Distinguished Young Scholars of China: 62225109