2020
DOI: 10.1364/boe.408790
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Defocused imaging exploits supercritical-angle fluorescence emission for precise axial single molecule localization microscopy: erratum

Abstract: We recently reported on the use of defocused imaging for single molecule localization microscopy close to the coverslip [Biomed. Opt. Express, 11, 775 (2020)10.1364/BOE.375678]. The original manuscript contains an error in the description of the Cramér-Rao lower bound (CRLB) calculations for SALM/DONALD, which affected the corresponding precision plot in Figure 2(b). We present a corrected description and plot.

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“…2 show 3D localization precisions for molecule positions ranging from 0 to 230 nm. The graphs are based on calculated Cramér-Rao lower bounds [ 33 , 47 , 48 ], assuming a UAF signal of 2000 photons and a background level of 100 photons per pixel. The best parameters obtained are stated above the graphs.…”
Section: Localization Performance Close To the Coverslipmentioning
confidence: 99%
“…2 show 3D localization precisions for molecule positions ranging from 0 to 230 nm. The graphs are based on calculated Cramér-Rao lower bounds [ 33 , 47 , 48 ], assuming a UAF signal of 2000 photons and a background level of 100 photons per pixel. The best parameters obtained are stated above the graphs.…”
Section: Localization Performance Close To the Coverslipmentioning
confidence: 99%