Model-based deep embedding for constrained clustering analysis of single cell RNA-seq data.

TLDR: Wang et al. as discussed by the authors proposed a principled clustering method named scDCC, which integrates domain knowledge into the clustering step to facilitate the biological interpretability of clusters, and subsequent cell type identification.

Abstract: Clustering is a critical step in single cell-based studies. Most existing methods support unsupervised clustering without the a priori exploitation of any domain knowledge. When confronted by the high dimensionality and pervasive dropout events of scRNA-Seq data, purely unsupervised clustering methods may not produce biologically interpretable clusters, which complicates cell type assignment. In such cases, the only recourse is for the user to manually and repeatedly tweak clustering parameters until acceptable clusters are found. Consequently, the path to obtaining biologically meaningful clusters can be ad hoc and laborious. Here we report a principled clustering method named scDCC, that integrates domain knowledge into the clustering step. Experiments on various scRNA-seq datasets from thousands to tens of thousands of cells show that scDCC can significantly improve clustering performance, facilitating the interpretability of clusters and downstream analyses, such as cell type assignment. Clustering cells based on similarities in gene expression is the first step towards identifying cell types in scRNASeq data. Here the authors incorporate biological knowledge into the clustering step to facilitate the biological interpretability of clusters, and subsequent cell type identification.