Fig. 3
- ID
- ZDB-FIG-160303-38
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- Stegmaier et al., 2016 - Real-Time Three-Dimensional Cell Segmentation in Large-Scale Microscopy Data of Developing Embryos
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Whole-Embryo Cell Segmentation in Fruit Fly, Zebrafish, and Mouse (A) Maximum-intensity projections of 3D image datasets of fruit fly, zebrafish, and mouse embryos expressing fluorescent markers labeling all membranes. Image data were acquired with light-sheet fluorescence microscopy (Tomer et al., 2012). The fruit fly embryo was imaged at 3 hr after egg laying (AEL), the zebrafish embryo at 6 hr post fertilization (hpf), and the mouse embryo at E6.5 (Experimental Procedures). Scale bar, 50 µm. (B) Segmentation results, visualized as renderings of sliced embryos. Cells in the exposed cross-sections are shown in an orange/red color scheme, and in a cyan/blue color scheme for the rest of the embryo. Insets show enlarged views of the cell segmentation results. (C) As in (A), but for fruit fly, zebrafish, and mouse embryos imaged with confocal fluorescence microscopy (Zeiss LSM 510 and LSM 710 microscopes). The fruit fly embryo was imaged at 3 hr AEL, the zebrafish embryo at 6 hpf, and the mouse embryo at E7.5 (Experimental Procedures). Scale bar, 50 µm. (D) Segmentation results for the image data shown in (C). |
Reprinted from Developmental Cell, 36, Stegmaier, J., Amat, F., Lemon, W.C., McDole, K., Wan, Y., Teodoro, G., Mikut, R., Keller, P.J., Real-Time Three-Dimensional Cell Segmentation in Large-Scale Microscopy Data of Developing Embryos, 225-240, Copyright (2016) with permission from Elsevier. Full text @ Dev. Cell