Single-cell RNA transcriptome data present a tremendous opportunity for studying the cellular heterogeneity. Identifying subpopulations based on scRNA-seq data is a hot topic in recent years, although many researchers have been focused on designing elegant computational methods for identifying new cell types; however, the performance of these methods is still unsatisfactory due to the high dimensionality, sparsity and noise of scRNA-seq data. In this study, we propose a new cell type detection method by learning a robust and accurate similarity matrix, named SCCLRR. The method simultaneously captures both global and local intrinsic properties of data based on a low rank representation (LRR) framework mathematical model. The integrated normalized Euclidean distance and cosine similarity are used to balance the intrinsic linear and nonlinear manifold of data in the local regularization term. To solve the non-convex optimization model, we present an iterative optimization procedure using the alternating direction method of multipliers (ADMM) algorithm. We evaluate the performance of the SCCLRR method on nine real scRNA-seq datasets and compare it with seven state-of-the-art methods. The simulation results show that the SCCLRR outperforms other methods and is robust and effective for clustering scRNA-seq data. (The code of SCCLRR is free available for academic https://github.com/wzhangwhu/SCCLRR).
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