Single-cell RNA sequencing (scRNA-seq) allows for the creation of large collections of individual cells transcriptome. Unsupervised clustering is an essential element for the analysis of these data, and it represents the initial step for the identification of different cell types to investigate the cell subpopulation structure of a biological sample. However, it is possible that the clustering aggregation features do not perfectly match the underlying biology since scRNA-seq data are characterized by high noise. In this chapter, we describe a functional feature-driven data reduction approach, which could provide a better link among cell clusters and their underlying cell biology.
Keywords: Data reduction; Kinase; Sparsely connected autoencoder; Transcription factor; miRNA.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.