http://imagej.273.s1.nabble.com/Re-Fiji-is-conventional-ImageJ-was-Make-images-overlap-tp3684283p3684284.html
From: JOEL B. SHEFFIELD <
convenient. I apologize for my poor choice of words --perhaps I should
have said "original", although that would ignore all of the upgrades, etc.
interested in specific projects that require a given plugin. For many new
rsb.nih.gov, or imagej.nih.gov, since that is where Google leads them.
> Hi Joel and all,
>
>
> On Jun 13, 2011, at 6:00 AM, IMAGEJ automatic digest system wrote:
>
> > Date: Sun, 12 Jun 2011 21:48:29 -0400
> > From: "JOEL B. SHEFFIELD" <
[hidden email]>
> > Subject: Re: Make images overlap
> >
> > It should also be possible to use the "Turbo Reg" plugin in conventional
> > ImageJ. You can search for it on the plugins page.
>
> But the point is, you dont need to bother to look for it, download it and
> install it manually.
>
> Just download fiji, update it and the latest StackReg version is already
> there ;-)
>
> Fiji is _not_ a competitor for ImageJ:
> Fiji IS just imageJ, with a bunch of stuff added on to make it nicer to
> use,
> eg the updater and much more.
>
> The same people all work together on ImageJ, ImageJA, ImageJ2, imglib and
> Fiji
>
> If anyone has a good reason to use plain ImageJ instead of the
> Fiji "distribution" of imageJ
> (that would be like building your own car from scratch, instead of buying a
> finished one)
> then we would really like to find out how and why,
> so we in the Fiji team can provide an ImageJ distribution that you _will_
> use.
>
> cheers
>
> Dan
>
>
>
> >
> > Joel
> >
> >
> > On Sun, Jun 12, 2011 at 5:45 PM, Stephan Saalfeld <
[hidden email]
> >wrote:
> >
> >> Hi Tomas,
> >>
> >> using Fiji, you have at least two options:
> >>
> >> 1.
> >> Open both images and mark corresponding points in both using the point
> >> selection tool (index number must match) and use the plugin:
> >>
> >>
http://pacific.mpi-cbg.de/wiki/index.php/Landmark_Correspondences> >>
> >> to map one image into the other using a transformation model of your
> >> choice (translation + rotation is rigid).
> >>
> >>
> >> 2.
> >> Import the slides into TrakEM2 and use either of the manual
> >> alignment/transformation modes. That is less trivial in terms of the
> >> learning the program and less easy to script but provides a much nicer
> >> user interface (interactive overlay supporting various overlay modes).
> >> The underlying engine is the same:
> >>
> >>
http://www.ini.uzh.ch/~acardona/trakem2_manual.html#transform_patch> >>
> >>
http://www.ini.uzh.ch/~acardona/trakem2_manual.html#landmarks> >>
> >> Good luck and best regards,
> >> Stephan
> >>
> >
>
> Dr. Daniel James White BSc. (Hons.) PhD
> Senior Microscopist / Image Processing and Analysis
> Light Microscopy Facility
> Max Planck Institute of Molecular Cell Biology and Genetics
> Pfotenhauerstrasse 108
> 01307 DRESDEN
> Germany
>
> +49 (0)15114966933 (German Mobile)
> +49 (0)351 210 2627 (Work phone at MPI-CBG)
> +49 (0)351 210 1078 (Fax MPI-CBG LMF)
>
>
http://www.bioimagexd.net BioImageXD
>
http://pacific.mpi-cbg.de Fiji (is just ImageJ - batteries
> included)
>
http://www.chalkie.org.uk>
[hidden email]
> (
[hidden email] )
>
>
>
>
>
>
>
Joel B. Sheffield, Ph.D
Joel B. Sheffield, Ph.D