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mmSIM: an open toolbox for accessible structured illumination microscopy
Author(s) -
Craig Russell,
Michael Shaw
Publication year - 2021
Publication title -
philosophical transactions of the royal society a mathematical physical and engineering sciences
Language(s) - English
Resource type - Journals
eISSN - 1471-2962
pISSN - 1364-503X
DOI - 10.1098/rsta.2020.0353
Subject(s) - toolbox , computer science , software , exploit , suite , process (computing) , synchronization (alternating current) , computer hardware , open source hardware , software engineering , open source , operating system , telecommunications , programming language , channel (broadcasting) , computer security , archaeology , history
Since the first practical super-resolution structured illumination fluorescence microscopes (SIM) were demonstrated more than two decades ago, the method has become increasingly popular for a wide range of bioimaging applications. The high cost and relative inflexibility of commercial systems, coupled with the conceptual simplicity of the approach and the desire to exploit and customize existing hardware, have led to the development of a large number of home-built systems. Several detailed hardware designs are available in the scientific literature, complemented by open-source software tools for SIM image validation and reconstruction. However, there remains a lack of simple open-source software to control these systems and manage the synchronization between hardware components, which is critical for effective SIM imaging. This article describes a new suite of software tools based on the popular Micro-Manager package, which enable the keen microscopist to develop and run a SIM system. We use the software to control two custom-built, high-speed, spatial light modulator-based SIM systems, evaluating their performance by imaging a range of fluorescent samples. By simplifying the process of SIM hardware development, we aim to support wider adoption of the technique. This article is part of the Theo Murphy meeting issue ‘Super-resolution structuredillumination microscopy (part 1)’.

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