CONFOCALMICROSCOPY Archives

January 1996

CONFOCALMICROSCOPY@LISTS.UMN.EDU

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

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

Print Reply
Sender:
Confocal Microscopy List <[log in to unmask]>
Subject:
From:
Peter Doerner <[log in to unmask]>
Date:
Fri, 12 Jan 1996 14:14:19 -0800
Reply-To:
Confocal Microscopy List <[log in to unmask]>
Parts/Attachments:
text/plain (18 lines)
                      Subject:                              Time:  14:08
  OFFICE MEMO         object recognition/quantitative...      Date:  01/12/96
 
Hi everyone,
 
We would like to quantitatively analyze confocal z-series of plant tissues. We
are examining organ primordia, with small, densely packed cells and would like
software to take the grudge out of two steps:
a) recognition of nuclei represented in several images of a stack;
b) quantitation of fluorescence within such a nuclear volume.
 
Is there software (preferably free) available to do this (Mac/PowerPC)?
 
Thanks for your time
peter and don
 
[log in to unmask]

ATOM RSS1 RSS2