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Hence, the loadings can be visualized and interpreted on a molecular level as pseudo 2D spectra in order to identify potential biomarkers.
Finally, the resulting reflectivity map can be visualized and interpreted.
In order to properly visualize the recorded reflections, the effect of the scan geometry must be compensated and the data must the migrated from the domain to the rectangular space where it will be visualized and interpreted.
Model results may be visualized and interpreted using MVAPACK routines that provide scatter and line plots of model scores and loadings in a variety of forms.
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In addition, the activation site (organ) can be visualized and identified.
The influence of these parameters and also time on axial velocity, pressure difference, maximum volumetric flow rate and streamline distributions (for elucidating trapping phenomena) is visualized graphically and interpreted in detail.
All materials were visualized and characterized by the Atomic Force Microcscopy (AFM) technique.
The crystal structures were visualized and prepared for calculations using Maestro10.3 (Schrödinger) with MacroModel10.9 (Schrödinger).
Reactions were quenched at various times and products were visualized and quantitated.
Section images were visualized and cells per field image counted using ImageJ software (NIH freeware).
DNA bands were visualized and quantified as described above.
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