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scCATCH: Automatic Annotation on Cell Types of Clusters from Single-Cell RNA Sequencing Data

Authors :
Xin Shao
Rui Xue
Xiaoyan Lu
Jie Liao
Xiaohui Fan
Ni Ai
Source :
iScience, Vol 23, Iss 3, Pp-(2020), iScience
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Summary Recent advancements in single-cell RNA sequencing (scRNA-seq) have facilitated the classification of thousands of cells through transcriptome profiling, wherein accurate cell type identification is critical for mechanistic studies. In most current analysis protocols, cell type-based cluster annotation is manually performed and heavily relies on prior knowledge, resulting in poor replicability of cell type annotation. This study aimed to introduce a single-cell Cluster-based Automatic Annotation Toolkit for Cellular Heterogeneity (scCATCH, https://github.com/ZJUFanLab/scCATCH). Using three benchmark datasets, the feasibility of evidence-based scoring and tissue-specific cellular annotation strategies were demonstrated by high concordance among cell types, and scCATCH outperformed Seurat, a popular method for marker genes identification, and cell-based annotation methods. Furthermore, scCATCH accurately annotated 67%–100% (average, 83%) clusters in six published scRNA-seq datasets originating from various tissues. The present results show that scCATCH accurately revealed cell identities with high reproducibility, thus potentially providing insights into mechanisms underlying disease pathogenesis and progression.<br />Graphical Abstract<br />Highlights • Construction of a comprehensive tissue-specific reference database of cell markers • Paired comparisons to identify potential marker genes for clusters to ensure accuracy • Evidence-based scoring and annotation for clustered cells from scRNA-seq data • Accurate and replicable annotation on cell types of clusters without prior knowledge<br />Quantitative Genetics; Cell Biology; Bioinformatics; Automation in Bioinformatics

Details

ISSN :
25890042
Volume :
23
Database :
OpenAIRE
Journal :
iScience
Accession number :
edsair.doi.dedup.....8f9f2a7960ada192725680843c888f57