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. 2023 Jul 6;55(7):1176–1185. doi: 10.1038/s41588-023-01435-6

Extended Data Fig. 1. Integration and cell-type annotation.

Extended Data Fig. 1

a. Brightfield images of representative embryos isolated from 3 independent foster mice and staged for the respective developmental stages. Scale bar, 500 µm. b. Distribution of beads profiled by Slide-seq from the respective stages. c. Violin plots showing the number of UMIs or genes recovered per bead. Log10 values are used to represent counts. UMI, unique molecular identifier. d. Violin plots showing the number of UMIs and genes recovered per bead across individual arrays. Log10 values are used to represent counts. UMI, unique molecular identifier. e. Uniform Manifold Approximation and Projection (UMAP) of Slide-seq data and 10X scRNA-seq reference atlas of mouse gastrulation26. The color of the beads corresponds to the predicted and annotated cell state. Inset: UMAP representation of beads covered by the indicated modalities (red). Each dot represents a bead or a cell. f. UMAP of integrated data from stages E6.5 to E9.5. Black beads represent cells/beads from the corresponding stage. Each dot represents a bead or a cell.