CIARA
CIARA identifies candidate marker genes for rare cell types in single-cell RNA sequencing and other single-cell omics data and integrates these candidates with clustering to improve detection and characterization of rare cell populations.
Key Features:
- Cluster-independent marker selection: Performs marker gene selection independently of pre-defined clusters to prioritize genes likely to mark rare cell types.
- Likelihood-based candidate selection: Selects and ranks candidate genes based on their likelihood of being markers for rare cell populations.
- Integration with clustering: Integrates selected candidate genes with conventional clustering algorithms to facilitate grouping and identification of rare cell types.
- Multi-omics applicability: Operates on single-cell RNA sequencing and other single-cell omics datasets.
- Enhanced rare-population detection: Improves detection and characterization of rare populations that standard clustering approaches may overlook.
Scientific Applications:
- Human gastrula analysis: Identified previously uncharacterized rare populations in human gastrula samples.
- Mouse embryonic stem cells: Detected rare populations in mouse embryonic stem cells treated with retinoic acid.
- General single-cell studies: Uncovers novel rare cell types overlooked by standard clustering in single-cell datasets.
Methodology:
CIARA selects candidate marker genes independently of clustering based on their likelihood of marking rare cell types and integrates these candidates with conventional clustering algorithms.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- library
- Programming Languages:
- R, Python
- Added:
- 1/26/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Lubatti G, Stock M, Iturbide A, Ruiz Tejada Segura ML, Riepl M, Tyser RCV, Danese A, Colomé-Tatché M, Theis FJ, Srinivas S, Torres-Padilla M, Scialdone A. CIARA: a cluster-independent algorithm for identifying markers of rare cell types from single-cell sequencing data. Development. 2023;150(11). doi:10.1242/dev.201264. PMID:37294170.