http://imagej.273.s1.nabble.com/soma-area-detection-tp3684897p3684900.html
Thank you for your suggestion. I am able to achieve better results with
.
the soma size. Any suggestions for filling the holes/nuclei in the grayscale
image before the reconstruction? Thanks in advance.
> Hi Quing,
>
> here is an attempt to translate the recipe into ImageJ commands:
>
> Top-hat with circular kernel of radius r:
> - duplicate the image
> Assuming that your foreground objects have higher pixel value
> than the background:
> - Process>Filters>Minimum on the copy, radius r, followed by
> - Process>Filters>Maximum on the copy, same radius r
> - Image calculator to subtract the copy from the original
> If your foreground pixel values are smaller than those of the background,
> exchange Min&Max, and subtract the original from the copy.
>
> Morphological opening:
> - Process>Filters>Minimum with radius r1 (smaller than r for the top-hat),
> then
> - Process>Filters>Maximum with the same radius r1
>
>
> Michael
> ________________________________________________________________
>
>
> On 19 Apr 2011, at 00:39, Qing Liu wrote:
>
> Dear all, I have found a solution to select neuronal soma but need your
>> suggestions to do so in imageJ.
>>
>>
http://dl.dropbox.com/u/266880/Soma.pdf>>
>> In the above paper, they mentioned
>>
>> the images of the neurons stained
>>
>>> for beta-III tubulin are first Gaussian filtered to suppress image
>>> noise. They are background corrected using a top hat morphological filter
>>> with a disk structuring element larger than the
>>> size of the largest cell body. A morphological opening
>>> with a structuring element of a diameter smaller than the cell
>>> body but larger than all neurites permits suppressing neuritelike
>>> structures.
>>>
>>>
>> I am a little confused about the second and third step and wonder if
>> anyone
>> can help.
>>
>> Thank you.
>>
>> Qing
>>
>