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A marker gene-based method for identifying the cell-type of origin from single-cell RNA sequencing data
- Source :
- MethodsX, Vol 10, Iss , Pp 102196- (2023)
- Publication Year :
- 2023
- Publisher :
- Elsevier, 2023.
-
Abstract
- Single-cell RNA sequencing (scRNA-seq) experiments provide opportunities to peer into complex tissues at single-cell resolution. However, insightful biological interpretation of scRNA-seq data relies upon precise identification of cell types. The ability to identify the origin of a cell quickly and accurately will greatly improve downstream analyses. We present Sargent, a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. We demonstrate Sargent's high accuracy by annotating simulated datasets. Further, we compare Sargent performance against expert-annotated scRNA-seq data from human organs including PBMC, heart, kidney, and lung. We demonstrate that Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. Additionally, the automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs. • Sargent is a transformation-free, cluster-free, single-cell annotation algorithm for rapidly identifying the cell types of origin based on cell type-specific markers. • Sargent retains both the flexibility and biological interpretability of cluster-based manual annotation. • Automation eliminates the labor intensive and potentially biased user annotation, producing robust, reproducible, and scalable outputs.
- Subjects :
- SARGENT - SignAtuRe-GEne cell aNnoTation
Science
Subjects
Details
- Language :
- English
- ISSN :
- 22150161
- Volume :
- 10
- Issue :
- 102196-
- Database :
- Directory of Open Access Journals
- Journal :
- MethodsX
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.b0bff18b1b40dda6c78781fb78cab5
- Document Type :
- article
- Full Text :
- https://doi.org/10.1016/j.mex.2023.102196