*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy*****
Hi there,
In the past I've used the Autoaligner module of Imaris that worked remarkably well!
Eric
Ps. No commercial interest!
**************PLEASE NOTE NEW ADRESS ************
Eric Scarfone, PhD
Research Scientist,
CNRS & Department of Neuroscience, Karolinska Institutet
Mob: +46 (0)70 888 2352
Visiting address:
Science for Life Laboratory,
Advanced Light Microscopy
Floor 1, room 1410
Tomtebodavägen 23A, Solna, Sweden
Postal address:
SciLifeLab
PO Box 1031
17121 Solna
Sweden
-----Original Message-----
From: Confocal Microscopy List [mailto:
[hidden email]] On Behalf Of Martin Wessendorf
Sent: 15 May 2012 03:12
To:
[hidden email]
Subject: Re: 3D reconstruction from serial sections
*****
To join, leave or search the confocal microscopy listserv, go to:
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy*****
Dear Manuel--
ImageJ (or better yet, its Fiji implementation) is probably the place to start, since it's free and there's a user listserv even more active than this one.
ImageJ (including its listserv) is found at:
http://rsbweb.nih.gov/ij/Fiji is at:
http://fiji.sc/wiki/index.php/FijiGood luck!
Martin Wessendorf
On 5/13/2012 10:13 PM, Manuel Pele wrote:
> *****
> To join, leave or search the confocal microscopy listserv, go to:
>
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> *****
>
> Hi everyone,
>
> I'm looking for a way to reconstruct a full 3D image of my samples
> that I need to image using serial sections. Any tips about which
> software I can use ? Does it work well?
>
> Cheers
>
> Manuel
>
--
Martin Wessendorf, Ph.D. office: (612) 626-0145
Assoc Prof, Dept Neuroscience lab: (612) 624-2991
University of Minnesota Preferred FAX: (612) 624-8118
6-145 Jackson Hall, 321 Church St. SE Dept Fax: (612) 626-5009
Minneapolis, MN 55455 e-mail:
[hidden email]
Locked
