SCISSORS
SCISSORS identifies rare cell types and subclusters in single-cell RNA sequencing (scRNA-seq) data by semi-supervised optimization of rare-cell silhouettes to improve detection of low-abundance populations within heterogeneous samples.
Key Features:
- Integration with Seurat R package: Integrates into Seurat-based scRNA-seq analysis workflows to operate on existing single-cell datasets and objects.
- Silhouette scoring: Employs silhouette scoring to estimate heterogeneity within clusters and to quantify cluster cohesiveness and separability.
- Semi-supervised reclustering: Uses a multi-step semi-supervised reclustering process to reveal rare cells within heterogeneous clusters.
- Marker gene identification: Identifies marker genes with high specificity for detected subclusters to support characterization of low-abundance cell populations.
Scientific Applications:
- Developmental biology: Resolves granular cellular heterogeneity and detects transient or low-abundance cell states in developmental scRNA-seq datasets.
- Cancer research: Identifies rare tumor subpopulations or microenvironmental cell types that may be masked in bulk clustering of scRNA-seq data.
- Immunology: Detects low-frequency immune cell subsets and refines subcluster definitions in heterogeneous immune profiling by scRNA-seq.
Methodology:
Integrates with the Seurat R package, applies silhouette scoring to estimate within-cluster heterogeneity, performs multi-step semi-supervised reclustering to reveal rare subclusters, and identifies marker genes specific to those subclusters.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- library
- Programming Languages:
- R
- Added:
- 1/2/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Leary JR, Xu Y, Morrison AB, Jin C, Shen EC, Kuhlers PC, Su Y, Rashid NU, Yeh JJ, Peng XL. <u>S</u>ub-<u>C</u>luster <u>I</u>dentification through <u>S</u>emi-<u>S</u>upervised <u>O</u>ptimization of <u>R</u>are-Cell <u>S</u>ilhouettes (SCISSORS) in single-cell RNA-sequencing. Bioinformatics. 2023;39(8). doi:10.1093/bioinformatics/btad449. PMID:37498558. PMCID:PMC10412410.