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Exploring Additional Valuable Information From Single-Cell RNA-Seq Data

期刊

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2020.593007

关键词

single-cell RNA-seq; cell-to-cell communication; RNA velocity; copy number variations; non-coding RNAs; cell-type deconvolution

资金

  1. National Natural Science Foundation of China [31771460, 32070680, 91629103]
  2. National Key Research and Development Program of China [2016YFC0902100]

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Single-cell RNA-seq (scRNA-seq) technologies are broadly applied to dissect the cellular heterogeneity and expression dynamics, providing unprecedented insights into single-cell biology. Most of the scRNA-seq studies mainly focused on the dissection of cell types/states, developmental trajectory, gene regulatory network, and alternative splicing. However, besides these routine analyses, many other valuable scRNA-seq investigations can be conducted. Here, we first review cell-to-cell communication exploration, RNA velocity inference, identification of large-scale copy number variations and single nucleotide changes, and chromatin accessibility prediction based on single-cell transcriptomics data. Next, we discuss the identification of novel genes/transcripts through transcriptome reconstruction approaches, as well as the profiling of long non-coding RNAs and circular RNAs. Additionally, we survey the integration of single-cell and bulk RNA-seq datasets for deconvoluting the cell composition of large-scale bulk samples and linking single-cell signatures to patient outcomes. These additional analyses could largely facilitate corresponding basic science and clinical applications.

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