Abstract
Single-cell RNA sequencing (scRNA-seq) is a powerful tool to study heterogeneity and dynamic changes in cell populations. Clustering scRNA-seq is essential in identifying new cell types and studying their characteristics. We develop CellBIC (single Cell BImodal Clustering) to cluster scRNA-seq data based on modality in the gene expression distribution. Compared with classical bottom-up approaches that rely on a distance metric, CellBIC performs hierarchical clustering in a top-down manner. CellBIC outperformed the bottom-up hierarchical clustering approach and other recently developed clustering algorithms while maintaining the hierarchical structure of cells. Importantly, CellBIC identifies type 2 diabetes and age specific β cell signatures characterized by SIX3 and CDH2, respectively.
| Originalsprog | Engelsk |
|---|---|
| Artikelnummer | e124 |
| Tidsskrift | Nucleic Acids Research |
| Vol/bind | 46 |
| Udgave nummer | 21 |
| Sider (fra-til) | 1-8 |
| Antal sider | 8 |
| ISSN | 0305-1048 |
| DOI | |
| Status | Udgivet - 2018 |
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