DendroSplit

DendroSplit provides interpretable clustering of single-cell RNA-Seq (scRNA-Seq) datasets to identify biologically meaningful cell populations.


Key Features:

  • Interpretability: Emphasizes interpretability, providing a framework to understand and justify clustering results from scRNA-Seq data.
  • Addressing Subjectivity: Implements a structured approach intended to reduce subjectivity and enhance reproducibility of clustering outcomes.
  • Feature selection and multi-level populations: Integrates feature selection to identify multiple levels of biologically meaningful populations aligned with definitions of "cell type".
  • Computational Efficiency: Demonstrates computational efficiency suitable for large-scale single-cell datasets.
  • Comparative Performance: Achieves clustering accuracy and speed comparable to existing methods while prioritizing interpretability.

Scientific Applications:

  • Single-cell genomics: Applied to analyze cellular heterogeneity in scRNA-Seq datasets.
  • Cell type and state identification: Used to identify distinct cell types and cell states from scRNA-Seq data.
  • Developmental biology: Facilitates resolution of cell-type heterogeneity in developmental studies.
  • Cancer research: Supports investigation of cellular heterogeneity relevant to cancer biology and disease mechanisms.
  • Immunology: Enables resolution of immune cell types and states in immunological studies.

Methodology:

Integrates feature selection into the clustering process to uncover biologically meaningful clusters at multiple levels.

Topics

Details

License:
CC-BY-4.0
Tool Type:
command-line tool
Operating Systems:
Linux, Mac
Programming Languages:
Python
Added:
8/6/2018
Last Updated:
12/10/2018

Operations

Data Inputs & Outputs

Publications

Zhang JM, Fan J, Fan HC, Rosenfeld D, Tse DN. An interpretable framework for clustering single-cell RNA-Seq datasets. BMC Bioinformatics. 2018;19(1). doi:10.1186/s12859-018-2092-7. PMID:29523077. PMCID:PMC5845381.

PMID: 29523077
PMCID: PMC5845381
Funding: - National Human Genome Research Institute: R01HG008164

Documentation