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When a single molecule is detected in a wide-field microscope, the image approximates the point spread function of the system. However, as the distribution of molecules becomes denser and their images begin to coincide, existing solutions to determine the number of molecules present and their precise three-dimensional locations can tolerate little to no overlap. A solution to this problem involving matched optical and digital techniques, as here proposed, is critical to increase the allowable labeling density and to accelerate single-molecule localization microscopy.

生成讲解博客的中文版本

生成AI智能校验的中文版本