Exact(8)
Trapped lysozyme microgel particles were also observed and imaged under the same imaging conditions as Ure2-AP microgel particles.
Both data sets were imaged with the same imaging setup such that results measured in pixels are comparable.
The fiber and chip are imaged using the exact same imaging system described above for the tapered fiber puller.
Cine, morphologic, and late gadolinium enhancement images acquired during the same imaging session were matched by slice position.
During the same imaging session, He spin density images were acquired using the same scanner and coil.
The same imaging parameters were used for all images acquired from all the groups compared.
These training images were captured using the same imaging protocol, and patients from the test and validation data sets did not overlap.
Consider a scenario in which users take images of root systems using the same imaging platform and setup.
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