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The data were then exported for further analyses in R. Image plots of each array were examined for spatial artifacts, and there was no evidence of systematic effects indicative of technical problems with the arrays.
All genes on the array were examined individually and ranked based on their power to discriminate GF versus CONV epithelia using cutoff points (P ≤ 0.05; number of neighbors = 10; number of predictor genes = 20) and support vector machine algorithms.
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Morphology of the dendrites array was examined by scanning electron microscopy.
The microneedle array was examined to verify that all of the MNs remained intact after insertion at different locations on the mouse skin, even after 15 insertions (Fig. 4).
The respective influences of orientation, chord and spacing of the louvers and the converging profile of the louver array are examined.
When a three-dimensional object or array is examined binocularly, the nearer points or objects require greater convergence for fixation than the more distant points or objects, so that this provides a cue to the three-dimensional character of the presentation.
Microstructure of the nanotip array was examined using SEM.
The morphology of the fabricated NC array was examined using field-emission scanning electron microscopy (SEM; S-4800, Hitachi, Ltd., Chiyoda-ku, Japan).
After anodization and annealing at 25 V and 350°C, respectively, the morphology of the highly ordered TiO2 nanotube array was examined by FE-SEM (Figure 2) to ascertain the nanotube dimensions.
Following hybridization each array was examined for quality.
The role of microtubules in organizing an asymmetric endomembrane array was examined by stabilizing microtubules with 5 μM paclitaxel (taxol) or depolymerizing microtubules with 5 μM oryzalin [ 31, 32].
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