Abstract
Super-resolution microscopy has revolutionized optical fluorescence imaging by improving 3D resolution by 1-2 orders of magnitude. While different methods can successfully increase the resolution, all methods share significant differences with standard imaging methods, making the usual measures of resolution inapplicable. In particular image quality and information content are spatially heterogeneous with variabilities that can be comparable to their mean values, limiting the use of the average resolution as a predictor for local information. A common use of super-resolution data is to test or establish structural models, and in these cases it would be valuable to assess the capacity of the data to validate a model. We focus here on single-molecule localization methods and present a new way of assessing the quality and reliability of super-resolution data.
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