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03_Methods.md

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Cells were assigned to cell groups using Monocle3 with UMAP clustering [1-11]. Data was normalized to remove batch effects using PCA clustering to 100 dimensions. Pseudotime was calculated in Monocle3, with colors representing pseudotime changes among the cell clusters. The top 3 marker genes expressed in each cluster were plotted with at least 10% of cells expressing the respective genes, using 10 cells as reference.  Bioinformatic methods for Monocle analyses can be found at: https://github.com/ISUgenomics/SingleCellRNAseq_RyanSmith.

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