GeneClust

GeneClust selects feature genes for single-cell RNA sequencing (scRNA-seq) cell clustering by optimizing gene relevance while minimizing redundancy and preserving complementarity.


Key Features:

  • Relevance Maximization: Evaluates gene expression profiles to prioritize genes that are highly informative for distinct cell types in scRNA-seq datasets.
  • Redundancy Minimization: Groups genes with similar expression patterns to reduce redundant features and improve clustering resolution.
  • Complementarity Preservation: Preserves complementary gene interactions to capture diverse biological processes within datasets.
  • Integration Capability: Designed as a plug-in, it integrates with existing cell clustering methods to supply selected feature genes for downstream clustering analyses.

Scientific Applications:

  • Enhanced Clustering Performance: Extensive benchmarking demonstrates significant improvements in the accuracy and reliability of scRNA-seq cell clustering when using GeneClust-selected features.
  • Investigation of Gene Interactions: Groups cofunctional genes involved in biological processes and pathways to facilitate study of gene interactions within specific cellular contexts.
  • Identification of Biologically Relevant Genes: Aids identification of genes pertinent to dataset-specific biological characteristics, supporting insight into cellular functions and disease mechanisms.

Methodology:

Groups genes by expression profiles, then selects a subset that maximizes relevance to cell types while minimizing redundancy and preserving complementarity among gene clusters.

Topics

Details

License:
AGPL-3.0
Cost:
Free of charge
Tool Type:
library
Operating Systems:
Mac, Linux, Windows
Programming Languages:
Python, R
Added:
3/20/2023
Last Updated:
11/24/2024

Operations

Publications

Deng T, Chen S, Zhang Y, Xu Y, Feng D, Wu H, Sun X. A cofunctional grouping-based approach for non-redundant feature gene selection in unannotated single-cell RNA-seq analysis. Briefings in Bioinformatics. 2023;24(2). doi:10.1093/bib/bbad042. PMID:36754847. PMCID:PMC10025445.

PMID: 36754847
Funding: - National Institutes of Health: R01GM122083, R01GM124061

Documentation