FIGURE 5 from Spectral Flow Cytometry Methods and Pipelines for Comprehensive Immunoprofiling of Human Peripheral Blood and Bone Marrow

crossref(2024)

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Dimensionality reduction to detect differences between PBMC donors. A–D, UMAP coordinates generated from concatenated data of live, non-red blood cell singlets and 85,000 lymphocytes (A), 100,000 CD45+ cells (B), 90,000 lymphocytes (C) or 5,000 monocytes (D) from each donor (n = 3). Plots on the left indicate clustering of cells in two-dimensional space; plots on the right show canonically gated major cell populations overlaid onto each UMAP. E–H, UMAP for each of 3 individual donors. T/B panel UMAPs (A and E); M/N/D panel total CD45+ cells UMAPs (B and F); M/N/D panel lymphocytes UMAPs (C and G); M/N/D panel monocytes UMAPs (D and H). Arrows (in E, F, G, and H) indicate examples of cell populations that differ in abundance between donor samples.

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