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Updated: Jul 24, 2025

Three-dimensional Super Resolution Microscopy of F-actin Filaments by Interferometric PhotoActivated Localization Microscopy iPALM
Published on: December 1, 2016
Current capabilities and future perspectives of FCS: super-resolution microscopy, machine learning, and in vivo
Jagadish Sankaran1, Thorsten Wohland2
1Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore, 138632, Singapore. jagadish_sankaran@gis.a-star.edu.sg.
Abstract:
Fluorescence correlation spectroscopy (FCS) is a single molecule sensitive tool for the quantitative measurement of biomolecular dynamics and interactions. Improvements in biology, computation, and detection technology enable real-time FCS experiments with multiplexed detection even in vivo. These new imaging modalities of FCS generate data at the rate of hundreds of MB/s requiring efficient data processing tools to extract information. Here, we briefly review FCS's capabilities and limitations before discussing recent directions that address these limitations with a focus on imaging modalities of FCS, their combinations with super-resolution microscopy, new evaluation strategies, especially machine learning, and applications in vivo.
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