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Journal ArticleDOI

Fourier ring correlation as a resolution criterion for super-resolution microscopy.

TLDR
It is shown that Fourier ring correlation provides an easy-to-use, laboratory consistent standard for measuring the resolution of SRM images, and is provided a freely available software tool that combines resolution measurement with image reconstruction.
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This article is published in Journal of Structural Biology.The article was published on 2013-09-01. It has received 288 citations till now. The article focuses on the topics: Resolution (electron density) & Near-field scanning optical microscope.

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Citations
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Journal ArticleDOI

Fast live-cell conventional fluorophore nanoscopy with ImageJ through super-resolution radial fluctuations.

TL;DR: The broad applicability of SRRF and its performance at low signal-to-noise ratios allows super-resolution using modern widefield, confocal or TIRF microscopes with illumination orders of magnitude lower than methods such as PALM, STORM or STED.
Journal ArticleDOI

Precisely and accurately localizing single emitters in fluorescence microscopy

TL;DR: A lucid synthesis of the developments on single-molecule localization precision and accuracy and their practical implications are presented in order to guide the increasing number of researchers using single-particle tracking and super-resolution localization microscopy.
Journal ArticleDOI

Quantitative evaluation of software packages for single-molecule localization microscopy

TL;DR: This work focuses on the computational aspects of super-resolution microscopy and presents a comprehensive evaluation of localization software packages, reflecting the various tradeoffs of SMLM software packages and helping users to choose the software that fits their needs.
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Three-Dimensional Localization of Single Molecules for Super-Resolution Imaging and Single-Particle Tracking

TL;DR: In this article, a variety of methods for obtaining both 3D super-resolution images and 3D tracking infers structures or motions extending in the axial direction can easily be missed or confused.
References
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Journal ArticleDOI

Imaging intracellular fluorescent proteins at nanometer resolution.

TL;DR: This work introduced a method for optically imaging intracellular proteins at nanometer spatial resolution and used this method to image specific target proteins in thin sections of lysosomes and mitochondria and in fixed whole cells to image retroviral protein Gag at the plasma membrane.
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Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM).

TL;DR: A high-resolution fluorescence microscopy method based on high-accuracy localization of photoswitchable fluorophores that can, in principle, reach molecular-scale resolution is developed.
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Ultra-High Resolution Imaging by Fluorescence Photoactivation Localization Microscopy

TL;DR: A new method for fluorescence imaging has been developed that can obtain spatial distributions of large numbers of fluorescent molecules on length scales shorter than the classical diffraction limit, and suggests a means to address a significant number of biological questions that had previously been limited by microscope resolution.
Journal ArticleDOI

The correlation averaging of a regularly arranged bacterial cell envelope protein

TL;DR: An adaptation of the ‘correlation averaging’ method is described which allows reliable and almost fully automatic image averaging in the case of near‐periodic structures notwithstanding the presence of substantial crystal imperfections.
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