Computer Aided Multicriterion Optimization System (CAMOS)

Author(s):  
Andrzej Osyczka
1992 ◽  
Vol 25 (28) ◽  
pp. 141-146
Author(s):  
M. Galopin ◽  
T-M. Dao ◽  
L. Lamarche

2019 ◽  
Vol 142 (7) ◽  
Author(s):  
Jikai Liu ◽  
Albert C. To

Abstract Conventional topology optimization presentations generally highlight the numerical and optimization details established on the specially customized discrete geometric modeling system, which is incompatible with the existing computer-aided design (CAD)/computer-aided engineering (CAE) systems. Therefore, tedious preprocessing and postprocessing are required to improve the editability and manufacturability, which are both time consuming and labor intensive. Hence, to address this challenging issue, a novel CAD-based topology optimization system is developed in this work. The following points are highlighted: (i) interoperability issue between CAD and topology optimization was addressed by using macro files to communicate the feature and modeling history information; then, (ii) structural shape and topology optimization is performed based on a B-spline-based approach, which inherits the original spline information from the upstream CAD model and of course, can return spline-based geometric information for optimized CAD model generation, and the last but the most important point to mention is that, (iii) modeling history was incorporated into the optimization process and dynamic modeling history change is enabled based on the optimality criteria. This final point is significant because history-based CAD modeling is still a main-stream approach, especially given the excellent postmodeling editability and design intent capture.


Author(s):  
Mark Ellisman ◽  
Maryann Martone ◽  
Gabriel Soto ◽  
Eleizer Masliah ◽  
David Hessler ◽  
...  

Structurally-oriented biologists examine cells, tissues, organelles and macromolecules in order to gain insight into cellular and molecular physiology by relating structure to function. The understanding of these structures can be greatly enhanced by the use of techniques for the visualization and quantitative analysis of three-dimensional structure. Three projects from current research activities will be presented in order to illustrate both the present capabilities of computer aided techniques as well as their limitations and future possibilities.The first project concerns the three-dimensional reconstruction of the neuritic plaques found in the brains of patients with Alzheimer's disease. We have developed a software package “Synu” for investigation of 3D data sets which has been used in conjunction with laser confocal light microscopy to study the structure of the neuritic plaque. Tissue sections of autopsy samples from patients with Alzheimer's disease were double-labeled for tau, a cytoskeletal marker for abnormal neurites, and synaptophysin, a marker of presynaptic terminals.


Author(s):  
Greg V. Martin ◽  
Ann L. Hubbard

The microtubule (MT) cytoskeleton is necessary for many of the polarized functions of hepatocytes. Among the functions dependent on the MT-based cytoskeleton are polarized secretion of proteins, delivery of endocytosed material to lysosomes, and transcytosis of integral plasma membrane (PM) proteins. Although microtubules have been shown to be crucial to the establishment and maintenance of functional and structural polarization in the hepatocyte, little is known about the architecture of the hepatocyte MT cytoskeleton in vivo, particularly with regard to its relationship to PM domains and membranous organelles. Using an in situ extraction technique that preserves both microtubules and cellular membranes, we have developed a protocol for immunofluorescent co-localization of cytoskeletal elements and integral membrane proteins within 20 µm cryosections of fixed rat liver. Computer-aided 3D reconstruction of multi-spectral confocal microscope images was used to visualize the spatial relationships among the MT cytoskeleton, PM domains and intracellular organelles.


2002 ◽  
Vol 38 (11) ◽  
pp. S39
Author(s):  
E Azavedo

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