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The process of segmenting the heart chambers and the great vessels will be followed by optimization of the model using CAD software.
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Stationary phase screening was followed by optimization of the modifier and injection solvent composition.
This was followed by optimization of the cell accelerator voltage (CAV); however, it was noticed that there was a possibility of cross talk between some compounds especially at low CAVs so this value was only optimized between two and seven.
This is followed by helmet optimization.
This design process is followed by shape optimization to improve stress-based local performance around hinges of the mechanism.
This is followed by an optimization procedure, using a variational formulation of active contours, that seeks to improve boundary mesh conformity to the zero level contour of the level set function.
The kinematic analysis is followed by an optimization process using the genetic algorithm method to determine the optimum length and orientation of the mechanism's members to minimize the variations of the toe, the camber and the caster angles.
A global alignment performed on all proteins was followed by local optimization of overlapping, sequential regions of protein in approximately fifty amino acid increments.
This was followed by the geometrical optimization of the cast part for minimum residual stresses.
The prescreening is followed by the MINLP optimization of the model.
Parametric studies are followed by the design optimization process to deduce key factors to inkjet head performance: nozzle geometry, droplet size, ejecting speed, pulse amplitude, and ink viscosity.
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CEO of Professional Science Editing for Scientists @ prosciediting.com