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Open AccessJournal ArticleDOI

Identifying and removing the cell-cycle effect from single-cell RNA-Sequencing data

Martin Barron, +1 more
- 27 Sep 2016 - 
- Vol. 6, Iss: 1, pp 33892-33892
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TLDR
Wang et al. as discussed by the authors presented ccRemover, a new method that reliably identifies the cell-cycle effect and removes it, which can serve as an important pre-processing step for many scRNA-Seq data analyses.
Abstract
Single-cell RNA-Sequencing (scRNA-Seq) is a revolutionary technique for discovering and describing cell types in heterogeneous tissues, yet its measurement of expression often suffers from large systematic bias. A major source of this bias is the cell cycle, which introduces large within-cell-type heterogeneity that can obscure the differences in expression between cell types. The current method for removing the cell-cycle effect is unable to effectively identify this effect and has a high risk of removing other biological components of interest, compromising downstream analysis. We present ccRemover, a new method that reliably identifies the cell-cycle effect and removes it. ccRemover preserves other biological signals of interest in the data and thus can serve as an important pre-processing step for many scRNA-Seq data analyses. The effectiveness of ccRemover is demonstrated using simulation data and three real scRNA-Seq datasets, where it boosts the performance of existing clustering algorithms in distinguishing between cell types.

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Journal ArticleDOI

A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications.

TL;DR: A practical guide to help researchers design their first scRNA-seq studies, including introductory information on experimental hardware, protocol choice, quality control, data analysis and biological interpretation is presented.
Journal ArticleDOI

High-throughput single-cell ChIP-seq identifies heterogeneity of chromatin states in breast cancer.

TL;DR: A single-cell chromatin immunoprecipitation followed by sequencing approach paves the way to study the role of chromatin heterogeneity, not just in cancer but in other diseases and healthy systems, notably during cellular differentiation and development.
Journal ArticleDOI

SingleCellNet: A Computational Tool to Classify Single Cell RNA-Seq Data Across Platforms and Across Species.

TL;DR: The tool, SingleCellNet, is described, which addresses issues and enables the classification of query single-cell RNA-seq data in comparison to reference single- CellNet data, and it is able to classify across platforms and species.
Journal ArticleDOI

Single-cell analysis of progenitor cell dynamics and lineage specification in the human fetal kidney

TL;DR: A comprehensive and dynamic gene expression profile of the developing human kidney at the single-cell level is provided and computational approaches infer developmental trajectories and interrogate the complex network of signaling pathways and cellular transitions.
Journal ArticleDOI

Single-Cell Transcriptomics Bioinformatics and Computational Challenges.

TL;DR: Current state-of-the-art bioinformatics tools and methods for scRNA-Seq analysis are reviewed, as well as addressing some critical analytical challenges that the field faces.
References
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Journal ArticleDOI

Exploration, normalization, and summaries of high density oligonucleotide array probe level data

TL;DR: There is no obvious downside to using RMA and attaching a standard error (SE) to this quantity using a linear model which removes probe-specific affinities, and the exploratory data analyses of the probe level data motivate a new summary measure that is a robust multi-array average (RMA) of background-adjusted, normalized, and log-transformed PM values.
Journal ArticleDOI

The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells

TL;DR: Monocle is described, an unsupervised algorithm that increases the temporal resolution of transcriptome dynamics using single-cell RNA-Seq data collected at multiple time points that revealed switch-like changes in expression of key regulatory factors, sequential waves of gene regulation, and expression of regulators that were not known to act in differentiation.
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