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Confocal scans were recorded with identical settings in each experiment and optical sections were set to 1.0 µm.
Assume identical settings as in [24].
Images were captured using identical settings and exposure time for each image.
For each foetus, the IVIM imaging sequence was repeated twice with identical settings.
Control data were obtained at the same time points in identical settings.
After exporting STL files, the Simplify 3D 4.0 (Simplify 3D) [25] slicer software was used to calculate the printing time under identical settings.
As described previously, there is a paucity of data testing APRV with identical settings, especially in clinical trials almost all of which were retrospective or crossover studies.
For analysis of colocalization using confocal microscopy, all images were acquired under identical settings using the Nikon Eclipse Ti confocal microscope.
The retrospective and bootstrap analyses use identical settings to the constant insolation scenario, with the one change being that they model fluctuations in the annual global insolation.
During this period, the GPS receivers of these satellites have identical settings, except for the updated tracking loops that are implemented on Swarm-C only.
Images were acquired and analyzed with identical settings.
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