Fig. 3: Cellular trajectories of neurological disorder risk genes in nonneuronal lineages. | Experimental & Molecular Medicine

Fig. 3: Cellular trajectories of neurological disorder risk genes in nonneuronal lineages.

From: An integrative single-cell atlas for exploring the cellular and temporal specificity of genes related to neurological disorders during human brain development

Fig. 3

UMAP visualization of estimated developmental lineages in the oligodendrocyte group (C0, C8, C9, and C38), colored by pseudotime (a) and developmental stage (b). c Distribution of cells by major cell type and clustering across pseudotime and temporal patterns of PDGFRA and OPALIN. d Expression profiles of neurological disorder risk genes across pseudotime for different lineages. e Functional annotations for early- and late-lineage cells with significantly enriched biological processes with multiple comparisons by FDR. f UMAP visualization of the estimated developmental lineage in the astrocyte group (C2 and C29). g Distribution of cells by developmental stage across pseudotime. h Expression profiles of neurological disorder risk genes across pseudotime for each lineage. i Distinct expression patterns of known astrocyte marker genes in each lineage. j Functional annotations for each lineage with significantly enriched biological processes with multiple comparisons by FDR.

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