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      Removal of subsurface fluorescence in cryo-imaging using deconvolution

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          Abstract

          We compared image restoration methods [Richardson-Lucy (RL), Wiener, and Next-image] with measured “scatter” point-spread-functions, for removing subsurface fluorescence from section-and-image cryo-image volumes. All methods removed haze, delineated single cells from clusters, and improved visualization, but RL best represented structures. Contrast-to-noise and contrast-to-background improvement from RL and Wiener were comparable and 35% better than Next-image. Concerning detection of labeled cells, ROC analyses showed RL ≈Wiener > Next-image >> no processing. Next-image was faster than other methods and less prone to image processing artifacts. RL is recommended for the best restoration of the shape and size of fluorescent structures.

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          Most cited references17

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          Method of obtaining optical sectioning by using structured light in a conventional microscope.

          We describe a simple method of obtaining optical sectioning in a conventional wide-field microscope by projecting a single-spatial-frequency grid pattern onto the object. Images taken at three spatial positions of the grid are processed in real time to produce optically sectioned images that are substantially similar to those obtained with confocal microscopes.
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            A workingperson's guide to deconvolution in light microscopy.

            Thefluorescence microscope is routinely used to study cellular structure in many biomedical research laboratories and is increasingly used as a quantitative assay system for cellular dynamics. One of the major causes of image degradation in the fluorescence microscope is blurring. Deconvolution algorithms use a model of the microscope imaging process to either subtract or reassign out-of-focus blur. A variety of algorithms are now commercially available, each with its own characteristic advantages and disadvantages. In this article, we review the imaging process in the fluorescence microscope and then discuss how the various deconvolution methods work. Finally, we provide a summary of practical tips for using deconvolution and discuss imaging artifacts and how to minimize them.
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              All-optical histology using ultrashort laser pulses.

              As a means to automate the three-dimensional histological analysis of brain tissue, we demonstrate the use of femtosecond laser pulses to iteratively cut and image fixed as well as fresh tissue. Cuts are accomplished with 1 to 10 microJ pulses to ablate tissue with micron precision. We show that the permeability, immunoreactivity, and optical clarity of the tissue is retained after pulsed laser cutting. Further, samples from transgenic mice that express fluorescent proteins retained their fluorescence to within microns of the cut surface. Imaging of exogenous or endogenous fluorescent labels down to 100 microm or more below the cut surface is accomplished with 0.1 to 1 nJ pulses and conventional two-photon laser scanning microscopy. In one example, labeled projection neurons within the full extent of a neocortical column were visualized with micron resolution. In a second example, the microvasculature within a block of neocortex was measured and reconstructed with micron resolution.
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                Author and article information

                Journal
                Opt Express
                Opt Express
                OE
                Optics Express
                Optical Society of America
                1094-4087
                11 October 2010
                07 October 2010
                : 18
                : 21
                : 22324-22338
                Affiliations
                [1 ]10900 Euclid Avenue, Wickenden Bldg, School of Biomedical Engineering, Cleveland OH 44106, USA
                [2 ]Department of Radiology, Case Western Reserve University and Case Medical Center, Cleveland OH 44106, USA
                Author notes
                Article
                133004
                10.1364/OE.18.022324
                3408948
                20941133
                5f64983d-d702-4580-a7fc-e9c8af028f8b
                ©2010 Optical Society of America

                This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.

                History
                : 6 August 2010
                : 12 September 2010
                : 20 September 2010
                Funding
                Funded by: Research Facilities Improvement Program
                Award ID: C06 RR12463-01
                Funded by: National Institutes of Health
                Award ID: R42CA124270
                Funded by: NIH
                Award ID: 1R24 CA110943
                Funded by: NIH
                Award ID: T32EB007509
                Categories
                Research-Article

                Ophthalmology & Optometry
                (180.2520) fluorescence microscopy,(170.3880) medical and biological imaging,(100.1830) deconvolution,(100.0100) image processing,(170.0170) medical optics and biotechnology,(180.0180) microscopy

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