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
nonlinear: scaling, e.g. with a gamma function
Would such a function include conversion from integer to float and back to
integer intensity values?
Guenter
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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
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