World's science and technologies have been challenged by the COVID‐19 pandemic. Each and every community across the globe are trying to find a real‐time novel method for accurate treatment and cure of COVID‐19 infected patients. The most important lead to take from this pandemic is to detect the infected patients as soon as possible and provide them an accurate treatment. At present, the worldwide methodology to detect COVID‐19 is reverse transcription‐polymerase chain reaction (RT‐PCR). This technique is costly and time taking. For this reason, the implementation of a novel method is required. This paper includes the use of deep learning analysis to develop a system for identifying COVID‐19 patients. Proposed technique is based on convolution neural network (CNN) and deep neural network (DNN). This paper proposes two models, first is designing DNN on the basis of fractal feature of the images and second is designing CNN using lungs x‐ray images. To find the infected area (tissues) of the lungs image using CNN architecture, segmentation process has been used. Developed CNN architecture gave results of classification with accuracy equal to 94.6% and sensitivity equal to 90.5% which is much better than the proposed DNN method, which gave accuracy 84.11% and sensitivity 84.7%. The outcome of the presented model shows 94.6% accuracy in detecting infected regions. Using this method the growth of the infected regions can be monitored and controlled. The designed model can also be used in post‐COVID‐19 analysis.
A b s t r a c t. The Cell Broadband Engine™ is a heterogeneous multi-core architecture developed by IBM, Sony and Toshiba. It has eight computation intensive cores (SPEs) with a small local memory, and a single PowerPC core. The SPEs have a total peak single precision performance of 204.8 Gflops/s, and 14.64 Gflops/s in double precision. Therefore, the Cell has a good potential for high performance computing. But the unconventional architecture makes it difficult to program. We propose an implementation of the core features of MPI as a solution to this problem. This can enable a large class of existing applications to be ported to the Cell. Our MPI implementation attains bandwidth up to 6.01 GB/s, and latency as small as 0.41 µs. The significance of our work is in demonstrating the effectiveness of intra-Cell MPI, consequently enabling the porting of MPI applications to the Cell with minimal effort.
Red blood cell biomechanics can provide us with a deeper understanding of macroscopic physiology and have the potential of being used for diagnostic purposes. In diseases like sickle cell anemia and malaria, reduced red blood cell deformability can be used as a biomarker, leading to further assays and diagnoses. A microfluidic system is useful for studying these biomechanical properties. We can observe detailed red blood cell mechanical behavior as they flow through microcapillaries using high-speed imaging and microscopy. Microfluidic devices are advantageous over traditional methods because they can serve as high-throughput tests. However, to rapidly analyze thousands of cells, there is a need for powerful image processing tools and software automation. We describe a workflow process using Image-Pro to identify and track red blood cells in a video, take measurements, and export the data for use in statistical analysis tools. The information in this protocol can be applied to large-scale blood studies where entire cell populations need to be analyzed from many cohorts of donors.
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