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.
Description
Current best practices in single-cell RNA-seq analysis: a tutorial. - PubMed - NCBI
%0 Journal Article
%1 Luecken:2019:Mol-Syst-Biol:31217225
%A Luecken, M D
%A Theis, F J
%D 2019
%J Mol Syst Biol
%K fulltext methods review rna-seq
%N 6
%R 10.15252/msb.20188746
%T Current best practices in single-cell RNA-seq analysis: a tutorial
%U https://www.ncbi.nlm.nih.gov/pubmed/31217225
%V 15
%X 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.
@article{Luecken:2019:Mol-Syst-Biol:31217225,
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.},
added-at = {2020-01-22T22:07:22.000+0100},
author = {Luecken, M D and Theis, F J},
biburl = {https://www.bibsonomy.org/bibtex/2b5a2d6c68c75e2094d59f62d50b90b14/marcsaric},
description = {Current best practices in single-cell RNA-seq analysis: a tutorial. - PubMed - NCBI},
doi = {10.15252/msb.20188746},
interhash = {63ab25e79e71bf601af0d0f2a70da7fb},
intrahash = {b5a2d6c68c75e2094d59f62d50b90b14},
journal = {Mol Syst Biol},
keywords = {fulltext methods review rna-seq},
month = {06},
number = 6,
pmid = {31217225},
timestamp = {2020-01-22T22:07:22.000+0100},
title = {Current best practices in single-cell RNA-seq analysis: a tutorial},
url = {https://www.ncbi.nlm.nih.gov/pubmed/31217225},
volume = 15,
year = 2019
}