http://imagej.273.s1.nabble.com/Reslice-stack-with-a-rotated-rectangular-selection-tp3692983p3692986.html
to lie between slices in your Z-stack. Output spacing controls how
>Thanks so much Bill,
>
>You just saved me many many hours and that was so so simple. It
>does raise one last question. What is the input Z spacing and
>output Z spacing? I can see the effects if I change those figures
>for myself but i dont understand what they are doing. The default
>for my image is 0.3um for both, but im not sure if this is just some
>kind of image J default or a default that is calculated from the
>image i open? Really the most important question is that im not
>sure what value is biologically relevent to my microscope
>image/cells, or whether there even is a biolgically relevent value i
>should be setting those parameters at? I dont want to unknowingly
>end up manipulating my data by setting parameters that I have no
>idea what they are actually doing and then not being able to explain
>myself.
>
>Any help from anyone on this would be appreciated.
>
>Mike
>
>----- Original Message ----- From: "Bill Mohler" <
[hidden email]>
>To: <
[hidden email]>
>Sent: Saturday, April 11, 2009 9:10 PM
>Subject: Re: Reslice stack with a rotated rectangular selection.
>
>>You should experiment with reslicing from a line selection. You can
>>start from any angle, and then define how far you want the slicing
>>to progress orthogonally.
>>
>>>Hey,
>>>
>>>Is there a plugin that will let me use the reslice command with a
>>>rectangular selection that I have rotated using
>>>edit>selection>rotate. When you rotate a rectangular selection
>>>reslice does not work anymore saying "line or rectangular
>>>selection required".
>>>
>>>The object im reslicing needs to be horizontal, and then i perform
>>>reslice from the top on my stack. I have about 50 cells im
>>>reslicing per field of view but all the cells are all at different
>>>angles. Currently im having to rotate my image constantly using
>>>image>rotate, getting each object im reslicing within the cell
>>>horizontal, then reslicing from the top with a normal rectangular
>>>selection. Im using interpolation when rotating my image. Is
>>>using interpolation and rotating many times a bad thing? the
>>>object im looking at after reslicing is only about 1.5 microns in
>>>diameter and is relatively close to the microscopes
>>>Z-sectioning/camera resolution.
>>>
>>>I should also say that i dont use imageJ extensively, and I do not
>>>know how to code, so if there is any options for what im trying to
>>>do Lehman's terms would be much appreciated.
>>>
>>>Thanks !
>>
>>
>>--
>>-----------------
>>William A. Mohler
>>Associate Professor
>>Dept. of Genetics and Developmental Biology
>>University of Connecticut Health Center
>>MC-3301
>>263 Farmington Ave.
>>Farmington, CT 06030-3301
>>
>>
[hidden email]
>>Mobile: (860) 985-2719
>>alt. mobile: (860) 331-8514
>>skype: wmohler
>>
>>Office: (860) 679-1833, room E2029
>>Lab: (860) 679-1834, room E2032
>>Fax: (314) 689-1833
>>
>>G&DB dept. ofc.: (860) 679-8350
>>G&DB dept. fax : (860) 679-8345
>>
http://genetics.uchc.edu/Faculty/Mohler/Mohler.html