Posted by
Glen MacDonald-2 on
URL: http://confocal-microscopy-list.275.s1.nabble.com/software-tp590473p590479.html
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocalHi Carl,
I've used this plugin for ImageJ. It does appear that one loses a
few gray levels in the end result, at least with this plugin and a
with commercial product to which it was compared.
http://rsb.info.nih.gov/ij/plugins/stack-focuser.htmlRegards,
Glen
Glen MacDonald
Core for Communication Research
Virginia Merrill Bloedel Hearing Research Center
Box 357923
University of Washington
Seattle, WA 98195-7923 USA
(206) 616-4156
[hidden email]
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The box said "Requires WindowsXP or better", so I bought a Macintosh.
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On Oct 5, 2007, at 4:34 PM, Carl Boswell wrote:
> Search the CONFOCAL archive at
>
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal>
> Dea all,
> Does anyone know of software that selects only in focus portions of
> an image and discards the out-of-focus parts. We need to get clear
> views of a curved surface (the fly eye) with a 10x objective using
> reflected light. Only thin optical slices are in focus at this
> mag, but if we could put together the portions that are in focus
> over the entire depth of the specimen, we could rebuild a clean
> image of the structure. This wouild be a used in an assay
> screening a bizillion flies, so SEM is not really practical.
> thanks,
> Carl
>
> Carl A. Boswell, Ph.D.
> Molecular and Cellular Biology
> University of Arizona
> 520-954-7053
> FAX 520-621-3709