High-resolution image reconstruction in fluorescence microscopy with patterned excitation
Applied Optics, Vol. 45, Issue 20, pp. 5037-5045 (2006)
http://dx.doi.org/10.1364/AO.45.005037
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Abstract
We discuss data treatment strategies in structured illumination microscopy, using simulated and experimental data. In the setup, the illumination pattern is generated by projecting a movable pinhole mask into the sample, and a wide-field fluorescence microscope image is acquired for each pattern position. The structured illumination data obtained from a two-dimensional illumination pattern can be treated by projection strategies such as in video confocal microscopy (sum, maximum, maximum minus minimum, and superconfocal), by a scaled subtraction of the out-of-focus estimate, or by a modified version of the Fourier-space treatment, as is known for data from one-dimensional structured illumination. We investigate the influence of some data processing strategies on unwanted effects such as residual patterning and local deviations from linearity in the reconstructed intensity.
© 2006 Optical Society of America
OCIS Codes
(070.2580) Fourier optics and signal processing : Paraxial wave optics
(100.3010) Image processing : Image reconstruction techniques
(100.6640) Image processing : Superresolution
(180.1790) Microscopy : Confocal microscopy
(180.2520) Microscopy : Fluorescence microscopy
History
Original Manuscript: August 24, 2005
Revised Manuscript: January 15, 2006
Manuscript Accepted: February 10, 2006
Virtual Issues
Vol. 1, Iss. 8 Virtual Journal for Biomedical Optics
Citation
Rainer Heintzmann and Pier A. Benedetti, "High-resolution image reconstruction in fluorescence microscopy with patterned excitation," Appl. Opt. 45, 5037-5045 (2006)
http://www.opticsinfobase.org/ao/abstract.cfm?URI=ao-45-20-5037
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