Oops, sorry, this was meant to go to the list, not (only) to the original
poster! ----- Weitergeleitet von Joachim Wesner/DEWET/LMSCentral/Leica am 15.05.2006 12:36 ----- |---------+----------------------------> | | Joachim Wesner | | | | | | 15.05.2006 11:59 | |---------+----------------------------> >------------------------------------------------------------------------------------------------------------------------------| | | | An: [hidden email] | | Kopie: | | Thema: Antwort: intensity correction of z stacks (linear, nonlinear)(Document link: Joachim Wesner) | >------------------------------------------------------------------------------------------------------------------------------| Hi, it seems such a plugin/capability does not yet exist, but it could be be implemented easily (albeit slow) in a macro. If I understand correctly, you only want to apply ONE scaling factor for each image of the stack that varies with z-depth/image#!? However, I would say a linear gradient is definitely not the way to go, a power law with a gamma may be, but what about exponential (as in an absorption model)?? On the other hand, a more elaborate correction would require a bit of knowledge of the objective, sample and microscope (pinhole etc.) data JW |---------+---------------------------------------> | | Guenter Giese | | | <Guenter.Giese@mpimf-heidelb| | | erg.mpg.de> | | | Gesendet von: ImageJ | | | Interest Group | | | <[hidden email]> | | | | | | | | | 15.05.2006 09:03 | | | Bitte antworten an | | | Guenter.Giese | |---------+---------------------------------------> >-------------------------------------------------------------------------------------------------------------------------------| | | | An: [hidden email] | | Kopie: (Blindkopie: Joachim Wesner/DEWET/LMSCentral/Leica) | | Thema: intensity correction of z stacks (linear, nonlinear) | >-------------------------------------------------------------------------------------------------------------------------------| Hi all, It is common in confocal microscopy that, despite of careful selection of embedding media, objectives etc., signal intensity drops with increasing focus depth (e.g in thick tissue samples). Is there any built-in function or a plugin available for intensity correction of z stacks (linear, nonlinear)? linear: scaling of intensities using a linear gradient of the scaling factor along the z axis nonlinear: scaling, e.g. with a gamma function along the z axis Does such a function include conversion from integer to float and back to integer intensity values? Scaling by maximizing contrast of individual image planes is not what I am looking for. Guenter ------------------------------------------ Dr. Guenter Giese Light Microscopy Facility Manager Dept. of Biomedical Optics MPI fuer Medizinische Forschung Jahnstr. 29 D-69120 Heidelberg, Germany Phone (+49) 6221-486-360 (Fax: -325) e-mail: [hidden email] http://lightmicro.mpimf-heidelberg.mpg.de ______________________________________________________________________ This email has been scanned by the MessageLabs Email Security System. For more information please visit http://www.messagelabs.com/email ______________________________________________________________________ |
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