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For both databases, the spectrograms are computed by using a resolution of 512 points.
Analysis of the prepared beads was performed using a resolution of 30× to determine the diameter of 10 randomly selected beads.
A total of 10 simulation runs were carried out with each run simulating for 3,600 s using a resolution of 8 time-steps per second.
The cephalometric analyses were performed digitally by means of the Radiocef Studio 2 program (Radiomemory Ltda, MG, Brazil), using a resolution of 300 dpi for the teleradiographs [9].
FT-IR studies were carried out in dispersive mode on thin film samples using Perkin Elmer FTIR spectrophotometer (model Spectrum RXI,UK), within a range of 400 4,400 cm−1 using a resolution of 4 cm−1.
For this purpose, the radiographs were digitized by a table scanner (Cranex D® Soredex Orion Corporation, Tuusula, Finland) [10], coupled to a transparency reader, using a resolution of 300 dpi, and saved in TIFF format (Tagged Image File Format) without compression.
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If you scan documents, you should use a resolution of no less than 600 ppi to yield a minimum of 6,000 pixels along the long axis.
Low magnification fluorescence microscopy uses a resolution of 500 µm to 1 mm and is used to monitor phenotypic effects on entire cell populations.
For MS/MS, we used a resolution of 17,500 at m/z 200, with an isolation window of 2 m/z.
For this study, we used a resolution of 10 μm in the z direction, which resulted in ~500 z-slices per kidney [ 21].
The μCT analysis performed by Mackenzie et al. [20] used a resolution of 5 μm, which although adequate for determining overall changes in cortical bone volume and porosity, was not sufficient to provide detailed information about the osteocyte lacunae.
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