EC-PGMGR

EC-PGMGR integrates multiple clustering methods with a probability graphical model and graph regularization to identify cell populations in single-cell RNA-seq (scRNA-seq) data.


Key Features:

  • Ensemble Clustering Approach: Combines more than two base clustering methods to produce integrated clustering results that capture complementary aspects of scRNA-seq data.
  • Probability Graphical Model (PGM) Integration: Employs a PGM to automatically determine the optimal number of clusters without requiring prior knowledge.
  • Graph Regularization: Incorporates a regularization term to mitigate the influence of weak base clustering results by assigning weights through a pre-learning process.
  • Self-Regulation Mechanism: Uses a self-regulating weighting scheme that enhances active clustering methods while diminishing the impact of less effective ones.
  • Performance Evaluation: Validated against four individual clustering methods and two other ensemble methods using Adjusted Rand Index (ARI) and Normalized Mutual Information (NMI).

Scientific Applications:

  • Cell type identification: Delineates cellular phenotypes and explores cellular heterogeneity from scRNA-seq datasets.
  • Robust clustering where cluster number is unknown: Provides ensemble-based clustering solutions for analyses that require automatic determination of cluster number and integration of multiple methods.

Methodology:

Assembles integrative results from base clustering methods in combination form with self-regulation weights via a pre-learning process; validated on seven datasets generated by various platforms containing between 822 and 5,132 single cells and compared to four individual clustering methods and two ensemble methods using ARI and NMI.

Topics

Details

Tool Type:
command-line tool
Programming Languages:
MATLAB
Added:
1/18/2021
Last Updated:
3/5/2021

Operations

Publications

Zhu Y, Zhang D, Zhang X, Yi M, Ou-Yang L, Wu M. EC-PGMGR: Ensemble Clustering Based on Probability Graphical Model With Graph Regularization for Single-Cell RNA-seq Data. Frontiers in Genetics. 2020;11. doi:10.3389/fgene.2020.572242. PMID:33329710. PMCID:PMC7673820.