【摘 要】
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In super-resolution localization microscopy (LM),fluorescence emission from densely labeled molecules is controlled to redistribute into thousands of camera frames,so that the positions of individual
【机 构】
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Britton Chance Center for Biomedical Photonics,Wuhan National Laboratory for Optoelectronics,Huazhon
【出 处】
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The 4th Advances in Optoelectronics and Micro/nano-optics (A
论文部分内容阅读
In super-resolution localization microscopy (LM),fluorescence emission from densely labeled molecules is controlled to redistribute into thousands of camera frames,so that the positions of individual molecules could be obtained precisely for the reconstruction of a final super-resolution image.Therefore,massive amounts of data need to be processed (including transfer,store,and analyze) in LM imaging,especially with the advantageous use of better-performing sCMOS cameras which offer simultaneously large field of view and extremely fast frame rates and thus generate up to 3.6 terabytes data in accumulative one-hour imaging.
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