Gary G. Li-2 |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Greetings: I am looking for software tools for tracking fluorescent particles in time series of z-stacks. Instead of the trajectories, I am more interested in fluctuation of the fluorescent intensities of the particles over time. Please share with me your experience and insight. Regards Gary G. Li, Ph.D. Microscopy Core Facility Manager NIH/NIDA, Baltimore, MD 21224 |
Sanghoon Oh |
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear Gary, Imaris can track particles in 3D. Also it can reconnect missing particles in certain time points, e.g. when the particle's brightness went down and did not acquired properly. Thanks. Sincerely, Sanghoon --------------------------------------------------- Sanghoon Oh, Ph.D. ([hidden email]) Memorial Sloan-Kettering Cancer Center Molecular Cytology Core Facility Tel.646-888-2186 --------------------------------------------------- -----Original Message----- From: Confocal Microscopy List [mailto:[hidden email]] On Behalf Of Gary G. Li Sent: Wednesday, March 21, 2012 1:05 PM To: [hidden email] Subject: Tracking particles in time series of z-stacks ***** To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Greetings: I am looking for software tools for tracking fluorescent particles in time series of z-stacks. Instead of the trajectories, I am more interested in fluctuation of the fluorescent intensities of the particles over time. Please share with me your experience and insight. Regards Gary G. Li, Ph.D. Microscopy Core Facility Manager NIH/NIDA, Baltimore, MD 21224 ===================================================================== Please note that this e-mail and any files transmitted from Memorial Sloan-Kettering Cancer Center may be privileged, confidential, and protected from disclosure under applicable law. If the reader of this message is not the intended recipient, or an employee or agent responsible for delivering this message to the intended recipient, you are hereby notified that any reading, dissemination, distribution, copying, or other use of this communication or any of its attachments is strictly prohibited. If you have received this communication in error, please notify the sender immediately by replying to this message and deleting this message, any attachments, and all copies and backups from your computer. |
John Oreopoulos |
In reply to this post by Gary G. Li-2
*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Hi Gary, There are a number of particle tracking plugins at the ImageJ plugins page: http://rsbweb.nih.gov/ij/plugins/index.html Here are a few: http://rsbweb.nih.gov/ij/plugins/tracker.html http://rsbweb.nih.gov/ij/plugins/multitracker.html http://bigwww.epfl.ch/sage/soft/spottracker/ http://www.imagescience.org/meijering/software/mtrackj/ I think if you use the following plugin with the basic tracker plugin, it will do what you want it to do (intensity measurements), but the other plugins listed above might also have the same feature built in already: http://rsbweb.nih.gov/ij/plugins/measure-track/index.html I haven't had much experience with these sorts of plugins, but given that there are so many, it seems to be a common type of measurement for others. Consider looking at the Fiji repository as well. John Oreopoulos On 2012-03-21, at 1:05 PM, Gary G. Li wrote: > ***** > To join, leave or search the confocal microscopy listserv, go to: > http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy > ***** > > Greetings: > I am looking for software tools for tracking fluorescent particles in time > series of z-stacks. Instead of the trajectories, I am more interested in > fluctuation of the fluorescent intensities of the particles over time. > Please share with me your experience and insight. > Regards > Gary G. Li, Ph.D. > Microscopy Core Facility Manager > NIH/NIDA, Baltimore, MD 21224 |
Free forum by Nabble | Edit this page |