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Comment
. 2016 Jun 9;34(6):591-3.
doi: 10.1038/nbt.3498.

The contribution of cell cycle to heterogeneity in single-cell RNA-seq data

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Comment

The contribution of cell cycle to heterogeneity in single-cell RNA-seq data

Andrew McDavid et al. Nat Biotechnol. .
No abstract available

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Figures

Figure 1
Figure 1
Correlations and pairwise relationships between principal components analysis (PCA) components 1–3, geometric library size, cell cycle (derived through Hoechst staining), and the scLVM latent factor in the mESC data set.

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References

    1. Buettner F, et al. Computational analysis of cell-to-cell heterogeneity in single-cell RNA-sequencing data reveals hidden subpopulations of cells. Nature Biotechnology. 2015;33:155–160. - PubMed
    1. McDavid A, et al. Modeling Bi-modality Improves Characterization of Cell Cycle on Gene Expression in Single Cells. PLoS Comput Biol. 2014;10:e1003696. - PMC - PubMed
    1. Risso D, Ngai J, Speed TP, Dudoit S. Normalization of RNA-seq data using factor analysis of control genes or samples. Nature Biotechnology. 2014;32:896–902. - PMC - PubMed
    1. Padovan-Merhar O, et al. Single mammalian cells compensate for differences in cellular volume and DNA copy number through independent global transcriptional mechanisms. Mol Cell. 2015;58:339–352. - PMC - PubMed
    1. Gagnon-Bartsch JA, Speed TP. Using control genes to correct for unwanted variation in microarray data. Biostatistics. 2012;13:539–552. - PMC - PubMed

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