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.
DOI: 10.1093/bib/bbad042
PMID: 36754847
PMCID: PMC10025445
Funding: - National Institutes of Health: R01GM122083, R01GM124061