CONFOCALMICROSCOPY Archives

March 2004

CONFOCALMICROSCOPY@LISTS.UMN.EDU

Options: Use Monospaced Font
Show Text Part by Default
Show All Mail Headers

Message: [<< First] [< Prev] [Next >] [Last >>]
Topic: [<< First] [< Prev] [Next >] [Last >>]
Author: [<< First] [< Prev] [Next >] [Last >>]

Print Reply
Subject:
From:
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Fri, 12 Mar 2004 07:50:05 +0100
Content-Type:
text/plain
Parts/Attachments:
text/plain (57 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Hi Daniel,
it is my opinion that the best commercial deconvolution software is  
Huygens (www.svi.nl). It is also possible to download XCOSM  for free.
IN both cases you have to deal with installation, machine power, some  
expertise etc...
In my LAB (www.lambs.it...still in progress but with some useful  
information) we decided to realize a web based service that is for free  
and that you can find at www.powermicroscope.com.
You simply have to send your images thorugh the web waiting for an  
e-mail that tells you when they are ready (we need more or less half a  
day depending on traffick.
Our program is completely automatic and this is the reason why for some  
periods it did not work: 1) failure of the computer where it is  
installed; 2) strange or funny image formats.

I do invite anyone to use it. I'd appreciate a feedback.

Software has been designed, written and implemented by a group of  
seniors and juniors (that did the dirty hard job!), namely: ALberto  
Diaspro, Patrizia Boccacci, Mario Bertero, Paola Bonetto, Giuseppe  
Vicidomini, Marco Scarito, Mattia Epifani, Mirko Davolio, Francesco Di  
Fato.

All my best
Alby


On Giovedė, mar 11, 2004, at 23:14 Europe/Rome, Daniel Amiot wrote:

> Greetings!
>  
> I am interested in deconvoluting my confocal Z-stacks.  I have done  
> deconvolution before, but only on epifluorescence microscope images.   
> I am using a Zeiss PASCAL system to create files with *.lsm  
> extensions.  What is the best software to use for this deconvolution  
> for confocal images?  And what shall I look for to differentiate  
> confocal vs. epifluorescence deconvolution?
>  
> Daniel M. Amiot II
> Department of Hypertension
> Case-Western Reserve University
> [log in to unmask]
>
........................................................................ 
....................................
... non basta, resistere, resistere...resistere
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
Alberto Diaspro
Department of Physics, University of Genoa
Via Dodecaneso 33, 16146 Genoa, Italy
voice: +39-0103536426/480  fax 010314218
[log in to unmask], http://www.lambs.it
http://wiley.com/cda/product/0,,0471409200,00.html

ATOM RSS1 RSS2