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. 2021 Mar 19;12:1748. doi: 10.1038/s41467-021-22002-9

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© The Author(s) 2021

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Fig. 1 — The various analyses performed on a single fluorescence data set are shown here: autocorrelation analysis to determine diffusion coefficient (top left), number and brightness analysis to determine particle brightness (top right), super-resolution radial fluctuations imaging to resolve structures (bottom left), and FCS diffusion law to determine sub-resolution protein organization (bottom right).