State-of-the-art light-sheet and confocal microscopes allow recording of entire embryos in 3D and over time (3D+t) for many hours. Fluorescently labeled structures can be segmented and tracked automatically in these terabyte-scale 3D+t images, resulting in thousands of cell migration trajectories that provide detailed insights to large-scale tissue reorganization at the cellular level. Here we present EmbryoMiner, a new interactive open-source framework suitable for in-depth analyses and comparisons of entire embryos, including an extensive set of trajectory features. Starting at the whole-embryo level, the framework can be used to iteratively focus on a region of interest within the embryo, to investigate and test specific trajectory-based hypotheses and to extract quantitative features from the isolated trajectories. Thus, the new framework provides a valuable new way to quantitatively compare corresponding anatomical regions in different embryos that were manually selected based on biological prior knowledge. As a proof of concept, we analyzed 3D+t light-sheet microscopy images of zebrafish embryos, showcasing potential user applications that can be performed using the new framework.

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New imaging techniques enable visualizing and analyzing a multitude of unknown phenomena in many areas of science at high spatio-temporal resolution. The rapidly growing amount of image data, however, can hardly be analyzed manually and, thus, future research has to focus on automated image analysis methods that allow one to reliably extract the desired information from large-scale multidimensional image data. Starting with infrastructural challenges, we present new software tools, validation benchmarks and processing strategies that help coping with large-scale image data. The presented methods are illustrated on typical problems observed in developmental biology that can be answered, e.g., by using time-resolved 3D microscopy images.

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