InterCellar

InterCellar predicts and analyzes cell–cell communication from single-cell transcriptomic (scRNA-seq) data to characterize ligand–receptor interactions and their associated biological pathways.


Key Features:

  • Predictive Analysis of Cell–Cell Communication: Uses computational algorithms to predict cellular interactions based on ligand–receptor expression dynamics inferred from scRNA-seq data.
  • Customized Biological Interpretation: Performs tailored analytical steps to enhance the biological interpretation of predicted interactions.
  • Multiple Visualization Options: Generates diverse visualizations to explore predicted interactions and their pathway associations.
  • Integration with Biological Pathways: Maps ligand–receptor interactions to biological pathways to contextualize cellular communication.
  • Data-Driven Comparative Analysis: Enables comparison of cell–cell communication patterns across different conditions for data-driven insights.

Scientific Applications:

  • COVID-19 analysis: Applied to study cellular communication patterns in COVID-19, identifying patterns of interaction and molecular signals.
  • Melanoma research: Applied to analyze cell–cell communication in melanoma to reveal interaction patterns and associated pathways.
  • Hypothesis generation: Supports generation of hypotheses about disease mechanisms and potential therapeutic targets by linking interactions to biological functions and pathways.

Methodology:

Predicts cell–cell interactions by analyzing ligand–receptor pairs identified in single-cell transcriptomic (scRNA-seq) data and links these interactions to biological pathway information.

Topics

Details

License:
MIT
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R
Added:
6/15/2022
Last Updated:
6/15/2022

Operations

Publications

Interlandi M, Kerl K, Dugas M. InterCellar enables interactive analysis and exploration of cell−cell communication in single-cell transcriptomic data. Communications Biology. 2022;5(1). doi:10.1038/s42003-021-02986-2. PMID:35017628. PMCID:PMC8752611.

Links