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.

PMID: 37294170
Funding: - Deutsche Forschungsgemeinschaft: CRC 1064, DFG STR 1385/5-1 - European Molecular Biology Organization: ALTF 383-2016 - Bundesministerium für Bildung und Forschung: 01IS18053A

Links