Parallel deconvolution of large 3D images obtained by confocal laser scanning microscopy
✍ Scribed by Piotr Pawliczek; Anna Romanowska-Pawliczek; Zbigniew Soltys
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 203 KB
- Volume
- 73
- Category
- Article
- ISSN
- 1059-910X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Various deconvolution algorithms are often used for restoration of digital images. Image deconvolution is especially needed for the correction of three‐dimensional images obtained by confocal laser scanning microscopy. Such images suffer from distortions, particularly in the Z dimension. As a result, reliable automatic segmentation of these images may be difficult or even impossible. Effective deconvolution algorithms are memory‐intensive and time‐consuming. In this work, we propose a parallel version of the well‐known Richardson–Lucy deconvolution algorithm developed for a system with distributed memory and implemented with the use of Message Passing Interface (MPI). It enables significantly more rapid deconvolution of two‐dimensional and three‐dimensional images by efficiently splitting the computation across multiple computers. The implementation of this algorithm can be used on professional clusters provided by computing centers as well as on simple networks of ordinary PC machines. Microsc. Res. Tech., 2010. © 2009 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES
Several assumptions are made when confocal scanning laser microscopy is used for the determination of the fractal dimension of aggregates. The purpose of this study is to experimentally show that one of these assumptions, which concerns the relation existing between the structure of an aggregate and
DNA ploidy provides important information for the evaluation of the prognosis of prostate cancer. For the purpose of DNA cytometry and nuclear measurements, we developed an image processing system for the acquisition and processing of three-dimensional (3D) images based on confocal scanning laser mi
A new p H indicator, seminaphthofluorescein (SNAFL)-calcein acetoxymethyl ester, was used for intracellular p H (pH,) measurement in living MDCK cells with a laser scanning confocal microscope (LSCM) equipped with an Argon/Krypton laser and dual-excitation and dual-emission (FITC/Texas Red) filter s