Search the CONFOCAL archive at
http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal

This question of cell tracking was adressed last year on the forum of
the Web site "Dynamic Cell Imaging" at www.univ-reims.fr/INSERM514/DCI

There were 13 contributors to the discussion.
I think you can find several elements of answer there.
But I also think that the "true" answer depends very much on your
experimental conditions, especially the density of cells you have in
your field of view.

Noel Bonnet

Judy Trogadis wrote:
> Search the CONFOCAL archive at
> http://listserv.acsu.buffalo.edu/cgi-bin/wa?S1=confocal
>
> Dear Confocalists,
>
> We are studying cell migration, as a result, I am interested  in any
> suggestions on various motion tracking software solutions for the
> analysis of cell movement on a time-lapse stack of images.
>
> Thank you
> Judy
>
>
> Judy Trogadis
> Bio-Imaging Coordinator
> St. Michael's Hospital, 7Queen
> 30 Bond St.
> Toronto, ON M5B 1W8
> Canada
> ph:  416-864-6060  x6337
> pager: 416-685-9219
> fax: 416-864-6043
> [log in to unmask]
>


--
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Pr Noël BONNET
INSERM Unit 514 and LERI (University of Reims)
Hôpital Maison Blanche
45, rue Cognacq Jay
51092 REIMS Cedex, France
Tel:(33) 3 26 78 77 71
Fax:(33) 3 26 06 58 61
Web pages:
INSERM U514: www.univ-reims.fr/INSERM514
LERI: www.univ-reims.fr/Labos/LERI
Personal: www.univ-reims.fr/INSERM514/bonnet/bonnet.html
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see also the WEB site "Dynamic Cell Imaging" at
http://www.univ-reims.fr/INSERM514/DCI
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