Current best practices in single-cell RNA-seq analysis: a tutorial.

Mol Syst Biol

Institute of Computational Biology, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany

Published: June 2019

AI Article Synopsis

  • * This text outlines a typical workflow for single-cell RNA-seq analysis, detailing essential pre-processing steps and downstream analyses, along with best-practice recommendations based on comparative studies.
  • * A practical case study is provided through a public dataset to demonstrate the workflow, making it a useful tutorial for both newcomers and seasoned researchers looking to refine their analysis methods.

Article Abstract

Single-cell RNA-seq has enabled gene expression to be studied at an unprecedented resolution. The promise of this technology is attracting a growing user base for single-cell analysis methods. As more analysis tools are becoming available, it is becoming increasingly difficult to navigate this landscape and produce an up-to-date workflow to analyse one's data. Here, we detail the steps of a typical single-cell RNA-seq analysis, including pre-processing (quality control, normalization, data correction, feature selection, and dimensionality reduction) and cell- and gene-level downstream analysis. We formulate current best-practice recommendations for these steps based on independent comparison studies. We have integrated these best-practice recommendations into a workflow, which we apply to a public dataset to further illustrate how these steps work in practice. Our documented case study can be found at https://www.github.com/theislab/single-cell-tutorial This review will serve as a workflow tutorial for new entrants into the field, and help established users update their analysis pipelines.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582955PMC
http://dx.doi.org/10.15252/msb.20188746DOI Listing

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