Abstract: The present disclosure provides a method and apparatus for scheduling a plurality of available graphics processing units (GPUs). Multiple GPU pools may be set, wherein each GPU pool is configured to serve one or more jobs requiring the same number of GPUs. Available GPUs may be assigned to each GPU pool. A job and job information related to the job may be received, wherein the job information indicates a number of GPUs required for performing the job. A corresponding GPU pool may be selected from the multiple GPU pools based at least on the job information. Available GPUs to be scheduled to the job in the selected GPU pool may be determined based at least on the job information. In addition, the determined available GPUs may be scheduled to the job.

Abstract: A lighting apparatus includes a first set of LED modules, a second set of LED modules, a first lens, a second lens and a driver. The first lens covers the first set of LED modules. The second lens covers the second set of LED modules. The driver supplies a first driving current and a second driving current respectively to the first set of LED module and the second set of LED modules. The driver electively turns on and turns off the first set of LED modules and the second set of LED modules in a first mode and in a second mode. The first light span in the first mode is partially overlapping the second light span in the second mode. The first light span has a smaller span angle than the second light span.

Abstract: A tissue microarray imaging system autonomously images, analyzes, and stores data for samples in a tissue microarray. The system may include a tissue microarray, a robotic microscope, and an imaging workstation that executes software to automatically control operation of the microscope to capture images from the microarray and analyze image results. A low magnification may be used to register samples within the microarray and obtain coordinates for each tissue specimen. Progressively higher magnifications may be used to analyze images of each registered specimen. Where multiple dyes are used to stain specimens, color separation techniques may be applied to independently measure and analyze each staining intensity. Images and quantitative data from the images may then be stored in a relational database for subsequent review. The system may be local, or may be Web-based for distributed control and sharing of results.

Abstract: The systems described herein autonomously image, analyze, and store date for samples in a tissue microarray. The system may include a tissue microarray, a robotic microscope, and an imaging workstation that executes software to automatically control operation of the microscope to capture images from the microarray and analyze image results. A low magnification may be used to register samples within the microarray and obtain coordinates for each tissue specimen. Progressively higher magnifications may be used to analyze images of each registered specimen. Images and quantitative data from the images may then be stored in a relational database for subsequent review. The system may be local, or may be Web-based for distributed control and sharing of results.

Abstract: The systems described herein autonomously image, analyze, and store date for samples in a tissue microarray. The system may include a tissue microarray, a robotic microscope, and an imaging workstation that executes software to automatically control operation of the microscope to capture images from the microarray and analyze image results. A low magnification may be used to register samples within the microarray and obtain coordinates for each tissue specimen. Progressively higher magnifications may be used to analyze images of each registered specimen. Images and quantitative data from the images may then be stored in a relational database for subsequent review. The system may be local, or may be Web-based for distributed control and sharing of results.

Abstract: A tissue microarray imaging system autonomously images, analyzes, and stores data for samples in a tissue microarray. The system may include a tissue microarray, a robotic microscope, and an imaging workstation that executes software to automatically control operation of the microscope to capture images from the microarray and analyze image results. A low magnification may be used to register samples within the microarray and obtain coordinates for each tissue specimen. Progressively higher magnifications may be used to analyze images of each registered specimen. Where multiple dyes are used to stain specimens, color separation techniques may be applied to independently measure and analyze each staining intensity. Images and quantitative data from the images may then be stored in a relational database for subsequent review. The system may be local, or may be Web-based for distributed control and sharing of results.