CONFOCALMICROSCOPY Archives

January 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:
Patty Jansma <[log in to unmask]>
Reply To:
Confocal Microscopy List <[log in to unmask]>
Date:
Fri, 23 Jan 2004 08:59:08 -0700
Content-Type:
text/plain
Parts/Attachments:
text/plain (44 lines)
Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

Hi, Gabor,

  You might want to check on the tracking software that has been developed 
by Compix. The website is www.cimaging.net and the phone number is (724) 
772-5277.


Patty Jansma
ARL Div of Neurobiology
University of AZ


At 11:32 AM 1/23/04 +0100, you wrote:
>Search the CONFOCAL archive at
>http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
>Dear All
>
>It is quite true that there are a number of softwares with which one can
>perform tracking. My main problem is that for the segmentation of the
>images these usually use tresholding which may work nicely for
>fluorescent images but fails often when phase contrast images of cell
>should be tracked. So my question is whether anyone is aware of a
>software with which one can automatically track phase contrast (or DIC)
>images of cells with minimal operator interference. Obviously in this
>case only in 2D...
>
>Thanks   Gabor
>
>--
>Gabor Csucs, PhD
>Light Microscopy Center
>Institute of Biochemistry
>Swiss Federal Institute of Technology, ETHZ
>
>tel     +41 1 633 6221
>        +41 1 633 6196                 ETH Hönngerberg
>fax     +41 1 633 1124                 CH-8093 Zürich
>email   [log in to unmask]
>www     http://www.biol.ethz.ch

ATOM RSS1 RSS2