Hi all,
I am trying to examine Ca2+ oscillations in time lapse images of cultured cells, specifically looking at the degree to which oscillations in neighbouring cells are synchronized. I have been able to use the Array.fourier() function to automate the analysis of the oscillation frequency (and ampltidue... I think). Is it possible to get the phase data from the Array.fourier() function somehow, or could the function be modified to get this information? Thanks, Damon -- Assistant Professor | Biomedical Physiology & Kinesiology | Simon Fraser University Member | Centre for Cell Biology, Development, and Disease | Simon Fraser University Tel: 778 782 9464 | Fax: 778 782 3040 | Office L8004 Mail to: Room K9625, 8888 University Drive, Burnaby BC V5A 1S6 http://www.sfu.ca/bpk/faculty_directory/poburko.html -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
Jay Unruh from Stowers has a plugin that does just what you want--you can
get those even in the updating website choices in IJ. It's called something like stack.temporal.FFT or similar, then follow that by complex.amp or complex.phase to extract what you want from the complex stack. He has Excel sheets describing all of the plugins. There is also a graphical description of the plugin in the supplemental of this paper: http://dx.doi.org/10.1016/j.molcel.2016.09.001 Jacob Keller On Wed, Dec 7, 2016 at 6:08 PM, Damon Poburko <[hidden email]> wrote: > Hi all, > > I am trying to examine Ca2+ oscillations in time lapse images of > cultured cells, specifically looking at the degree to which oscillations in > neighbouring cells are synchronized. I have been able to use the > Array.fourier() function to automate the analysis of the oscillation > frequency (and ampltidue... I think). > > Is it possible to get the phase data from the Array.fourier() function > somehow, or could the function be modified to get this information? > > Thanks, > Damon > > -- > > Assistant Professor | Biomedical Physiology & Kinesiology | Simon Fraser > University > Member | Centre for Cell Biology, Development, and Disease | Simon Fraser > University > Tel: 778 782 9464 | Fax: 778 782 3040 | Office L8004 > Mail to: Room K9625, 8888 University Drive, Burnaby BC V5A 1S6 > http://www.sfu.ca/bpk/faculty_directory/poburko.html > > > -- > ImageJ mailing list: http://imagej.nih.gov/ij/list.html > -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
In reply to this post by dpoburkoSFU
Good day Damon,
you may have a look at "nr realft" <http://www.gluender.de/Miscellanea/MiscTexts/UtilitiesText.html> described here: <http://www.gluender.de/Miscellanea/MiscTexts/MiscExcerpts /ReadMe_FFT.html> Best Herbie :::::::::::::::::::::::::::::::::::::::::: Am 08.12.16 um 00:08 schrieb Damon Poburko: > Hi all, > > I am trying to examine Ca2+ oscillations in time lapse images of > cultured cells, specifically looking at the degree to which oscillations > in neighbouring cells are synchronized. I have been able to use the > Array.fourier() function to automate the analysis of the oscillation > frequency (and ampltidue... I think). > > Is it possible to get the phase data from the Array.fourier() > function somehow, or could the function be modified to get this > information? > > Thanks, > Damon > -- ImageJ mailing list: http://imagej.nih.gov/ij/list.html |
Free forum by Nabble | Edit this page |