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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hugin works well for 2d. Peter > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Does anyone have a favorite free/shareware image stitching program they'd like to share? I have never attempted it in ImageJ either, is there a plug in? > > I am only trying to stitch together a few images right to left, not in both directions. > > Thanks for anything you have to share. > > Christian |
In reply to this post by Pedro Almada
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** On 15.11.2010 20:37, Pedro Almada wrote: > > I've had great success with the 2D/3D stitching plugin for ImageJ that is > included in the FIJI package: > http://pacific.mpi-cbg.de/wiki/index.php/Stitching_2D/3D > I second that. I use this plugin in "normal" ImageJ, 64bit-Windows. Stitching 200 MB 3D stacks together is not a problem. I didn't have a case where it wouldn't work if the edges to be stiched where marked as ROI. In many cases it also works without ROIs but for stacks it then takes noticeably longer and needs more RAM. The only drawback is that the stiching-plugin is not compatible with newer versions of the LOCI Bioformatimporters, i.e. if both are installed LOCI doesn't work while stitching does. (so you have to get the stitching folder out of your plugins folder and restart ImageJ to bioimport.) Steffen -- ------------------------------------------------------------ Steffen Dietzel, PD Dr. rer. nat Ludwig-Maximilians-Universität München Walter-Brendel-Zentrum für experimentelle Medizin (WBex) Head of light microscopy Mail room: Marchioninistr. 15, D-81377 München Building location: Marchioninistr. 27, München-Großhadern |
In reply to this post by Mario Emmenlauer
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** I will check it out, along with FIJI the ImageJ package. Thanks for all the input. --- On Tue, 11/16/10, Mario Emmenlauer <[hidden email]> wrote: From: Mario Emmenlauer <[hidden email]> Subject: Re: image stitching To: [hidden email] Date: Tuesday, November 16, 2010, 1:32 AM ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi, On 11/15/2010 08:46 PM, Mark Cannell wrote: > > See also: > > http://www.xuvtools.org/doku.php XuvTools is neat because it can work manual or fully automatic, so you can always fine-tune if something goes wrong. The newest version (beta) can also read files via Bio-Formats library, so its worth looking at. It will only stitch "real" 3D though, so stacks with more than 4 planes. Thats a bug that the developers (meaning 'me') meant to fix for quite a while now... All the best, Mario > Cheers > > On 16/11/2010, at 8:37 AM, Pedro Almada wrote: >> >> >> I've had great success with the 2D/3D stitching plugin for ImageJ that is >> included in the FIJI package: >> http://pacific.mpi-cbg.de/wiki/index.php/Stitching_2D/3D >> >> On 15 November 2010 19:35, Cammer, Michael <[hidden email]>wrote: > >> sts.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> If you have Photoshop CS3 or more recent, it has a nice Photomerge option >>> in the File menu. >>> -Michael >>> >>> -----Original Message----- >>> From: Confocal Microscopy List [mailto:[hidden email]] >>> On Behalf Of Christian >>> Sent: Monday, November 15, 2010 2:33 PM >>> To: [hidden email] >>> Subject: image stitching >>> >>> ***** >>> To join, leave or search the confocal microscopy listserv, go to: >>> http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >>> ***** >>> >>> Does anyone have a favorite free/shareware image stitching program they'd >>> like to share? I have never attempted it in ImageJ either, is there a plug >>> in? >>> >>> I am only trying to stitch together a few images right to left, not in both >>> directions. >>> >>> Thanks for anything you have to share. >>> >>> Christian >>> >>> ------------------------------------------------------------ >>> This email message, including any attachments, is for the sole use of the >>> intended recipient(s) and may contain information that is proprietary, >>> confidential, and exempt from disclosure under applicable law. Any >>> unauthorized review, use, disclosure, or distribution is prohibited. If you >>> have received this email in error please notify the sender by return email >>> and delete the original message. Please note, the recipient should check >>> this email and any attachments for the presence of viruses. The organization >>> accepts no liability for any damage caused by any virus transmitted by this >>> email. >>> ================================= >>> > |
In reply to this post by Christian-103
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To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Stitchers, On Nov 17, 2010, at 7:01 AM, CONFOCALMICROSCOPY automatic digest system wrote: > > Date: Tue, 16 Nov 2010 16:48:31 +0100 > From: Steffen Dietzel <[hidden email]> > Subject: Re: image stitching > > > On 15.11.2010 20:37, Pedro Almada wrote: >> >> I've had great success with the 2D/3D stitching plugin for ImageJ that is >> included in the FIJI package: >> http://pacific.mpi-cbg.de/wiki/index.php/Stitching_2D/3D >> > > I second that. I use this plugin in "normal" ImageJ, 64bit-Windows. > Stitching 200 MB 3D stacks together is not a problem. I didn't have a > case where it wouldn't work if the edges to be stiched where marked as > ROI. In many cases it also works without ROIs but for stacks it then > takes noticeably longer and needs more RAM. > > The only drawback is that the stiching-plugin is not compatible with > newer versions of the LOCI Bioformatimporters, i.e. if both are > installed LOCI doesn't work while stitching does. (so you have to get > the stitching folder out of your plugins folder and restart ImageJ to > bioimport.) > If you use Fiji instead of naked imageJ it is much more likely to work, as thats the context it is developed and tested in. Before stuff goes into the Fiji updater, it gets tested by the developers agains the currently bundled versions of imageJ(A), bio-formats, etc. If you have a reason to use naked ImageJ instead of Fiji, we would sure like to hear about it!!! There should ber nothing that you can do in naked imageJ that cant be done as well or better in Fiji. (Remember ----- Fiji is just imageJ - batteries included ---- its not a real fork or alternative software, its the same thing with nice stuff added.) Just let us know what the issue is and we can work towards resolving it. Fiji has many usability advantages over naked imageJ, which you should find useful. If not, please tell us why. cheers Dan > Steffen > > -- > ------------------------------------------------------------ > Steffen Dietzel, PD Dr. rer. nat > Ludwig-Maximilians-Universität München > Walter-Brendel-Zentrum für experimentelle Medizin (WBex) > Head of light microscopy > > Mail room: > Marchioninistr. 15, D-81377 München > > Building location: > Marchioninistr. 27, München-Großhadern Dr. Daniel James White BSc. (Hons.) PhD Senior Microscopist / Image Visualisation, Processing and Analysis Light Microscopy and Image Processing Facilities 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 Dan's Homepages https://ifn.mpi-cbg.de Dresden Imaging Facility Network dan (at) chalkie.org.uk ( white (at) mpi-cbg.de ) |
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