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Morphodynamic maps of cell movements for all tissues superimposed in embryo A (left), shown side-by-side with the maps representing average cellular dynamics across four different embryos (right). Note that the average morphodynamics map is only defined for the developmental stages captured in the image data of all four contributing embryos and thus starts a bit later (10:30:00) than the map for embryo A alone. Dramatic changes in tissue movements can be seen between the streak stages, when cell
⏲ 41 sec ✓ 26-Sep-2018
Thermosense Limited
⏲ 40 seconds 👁 1.3K
Bryce Energy Services
⏲ 44 minutes 41 seconds 👁 83
Visualization of embryo shown in Movie S2, superimposed with colored spots marking cell divisions automatically detected by a convolutional neural network in the three-dimensional image data over time. Precision and recall of the detector are 0.81/0.81 for the threshold setting used in this visualization, i.e. 81% of all detections shown in this video are true cell divisions, and 81% of all divisions occurring in the embryo were correctly retrieved by the neural network. This corresponds to a de
⏲ 51 sec ✓ 26-Sep-2018
Tony St John
⏲ 9 minutes 7 seconds 👁 96.1K
Syed Shah Zahurullah Hussaini
⏲ 5 minutes 45 seconds 👁 178K
Side-by-side comparison of a dual-expressing H2B-eGFP and T-mCherry embryo developing from an EB to early somite stage (left panel, distal view maximum-intensity projection) and a rendering of cell objects in the average embryo (right panel, distal view). The T-mCherry positive region from the image data was mapped onto the average embryo at a single time point (24.5 h) and then propagated backwards and forwards in time with the SVF data of cell tracks in the average embryo. Note that the develo
⏲ 27 sec ✓ 26-Sep-2018
Bryce Energy Services
⏲ 8 minutes 44 seconds 👁 17
Excel, Word and PowerPoint Tutorials from Howtech
⏲ 1 minute 5 seconds 👁 63.9K
Embryo-wide reconstruction of cell fates as a function of time in development. The reconstruction was performed by (1) manually labeling tissues in the image data at the last time point of the time-lapse recording and (2) using SVF-enhanced cell tracking to propagate these labels backward in time to trace cell fates to their developmental origin. Distal and lateral views of the developing embryo are shown with different tissues represented as differently colored SVF-tracked objects. Time is repr
⏲ 23 sec ✓ 26-Sep-2018
DSCOVR Analytics
⏲ 5 minutes 35 seconds 👁 1.8K
Aja Kitchen
⏲ 38 seconds 👁 111.6M
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