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. Author manuscript; available in PMC: 2020 May 2.
Published in final edited form as: Cell Stem Cell. 2019 Apr 11;24(5):707–723.e8. doi: 10.1016/j.stem.2019.03.006

Figure 1. Unsupervised ordering of the hGFAP-GFP-derived cells reveals developmental hierarchy.

Figure 1.

(A) Scheme for analysis of hGFAP-GFP+ cells using scRNA-seq from neonatal cortices (n=5 mice).

(B) t-SNE analysis of hGFAP-GFP+ cell clusters.

(C) Heatmap of hGFAP-GFP+ cells ordered as t-SNE (n = 815). Columns, individual cells; rows, genes.

(D) The proportions of distinct clusters among total hGFAP-GFP+ cells.

(E) Dot plot of levels of selected marker genes in subpopulations.

(F-G) t-SNE plots of F) astrocyte (Astro), radial glia (RG), and iGC and G) marker genes.

(H) Comparison of astrocyte and iGC clusters with adult astrocyte populations.

(I-J) t-SNE plot of I) OPC and pri-OPC cells and J) marker genes.

(K) Pseudo-time ordering of pri-OPCs and OPCs in hGFAP-GFP+ dataset. Red line, the predicted trajectory.

(L) Predicted lineage trajectories from RG-like cells in hGFAP-GFP+ cells.

See also Figure S1 and Table S2.