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Motivation Since the development of single-cell RNA sequencing (scRNA-seq) technologies, clustering analysis of single-cell gene expression data has been an essential tool for distinguishing cell types and identifying novel cell types. Even though many methods have been available for scRNA-seq clustering analysis, the majority of them are constrained by the requirement on predetermined cluster numbers or the dependence on selected initial cluster assignment. Results In this article, we propose an adaptive embedding and clustering method named scAce, which constructs a variational autoencoder to simultaneously learn cell embeddings and cluster assignments. In the scAce method, we develop an adaptive cluster merging approach which achieves improved clustering results without the need to estimate the number of clusters in advance. In addition, scAce provides an option to perform clustering enhancement, which can update and enhance cluster assignments based on previous clustering results from other methods. Based on computational analysis of both simulated and real datasets, we demonstrate that scAce outperforms state-of-the-art clustering methods for scRNA-seq data, and achieves better clustering accuracy and robustness. Availability and implementation The scAce package is implemented in python 3.8 and is freely available from https://github.com/sldyns/scAce. [ABSTRACT FROM AUTHOR]

Motivation Single-cell RNA sequencing technologies facilitate the characterization of transcriptomic landscapes in diverse species, tissues and cell types with unprecedented molecular resolution. In order to better understand animal development, physiology, and pathology, unsupervised clustering analysis is often used to identify relevant cell populations. Although considerable progress has been made in terms of clustering algorithms in recent years, it remains challenging to evaluate the quality of the inferred single-cell clusters, which can greatly impact downstream analysis and interpretation. Results We propose a bioinformatics tool named Phitest to analyze the homogeneity of single-cell populations. Phitest is able to distinguish between homogeneous and heterogeneous cell populations, providing an objective and automatic method to optimize the performance of single-cell clustering analysis. Availability and implementation The PhitestR package is freely available on both Github (https://github.com/Vivianstats/PhitestR) and the Comprehensive R Archive Network (CRAN). There is no new genomic data associated with this article. Published data used in the analysis are described in detail in the Supplementary Data. Supplementary information Supplementary data are available at Bioinformatics online. [ABSTRACT FROM AUTHOR]