Difference between revisions of "Microphotography"

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=Taking the picture=
=Taking the picture=
==Key to good pictures==
==The keys to good pictures==
*Spend time on set-up.
*Spend time on set-up.
**Clean the slide.
**Clean the slide.
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**Put normal beside pathologic - so one has a reference point.
**Put normal beside pathologic - so one has a reference point.
***Transititions are usually interesting.
***Transititions are usually interesting.
**Use the ''rule of thirds''.
**Where to put the centre of interest:
***Truly beautiful: use the ''rule of thirds'' - see ''[[Microphotography#Composition|composition section]]''.
***Functional: centre of interest in the centre.
*Focus.
*Focus.
**Sharpness of nuclear membrane and detail in the cytoplasm.
**Sharpness of nuclear membrane and detail in the cytoplasm.
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*[[De-vignetting]].
*[[De-vignetting]].
*Pictures at different magnification.
*Pictures at different magnification.
**Several are better than one.
**Sets are usually better than one.
**Many entities have high and low power features.
**Many entities have high and low power features.
***If is often impossible to capture them with one picture.
***It is often impossible to capture them with one picture.


==Camera settings==
==Camera settings==
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==Composition==
==Composition==
*The centre of interest, usually, should be at the centre.
[[Image:Rivertree thirds md.gif|thumb|150px|A picture that uses the ''rule of thirds''. (WC)]]
**An artsy look can be achieved by making use of the rule-of-thirds.
Functional pictures that tell a story and are easy to understand:
***Rule-of-thirds: centre of interest is at one of the four intersects of the imaginary lines that divide the image into thirds.
*The centre of interest at the centre.
 
An artsy look can be achieved by making use of the [[Wikipedia:Rule_of_thirds|rule of thirds]].
*Rule of thirds: centre of interest is at one of the four intersects of the imaginary lines that divide the image into thirds.


=Post-processing=
=Post-processing=
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Some random notes:
Some random notes:
*Software for microscope cameras usually have de-vignetting tools.  The tools go by different names and usually entail taking a background image.  Ideally, one should shoot the background image at the same magnification as the (primary) image.
*Vignetting is usually worse at lower magnification.
Random links:
*[http://www.gimp.org/release-notes/gimp-2.4.html http://www.gimp.org/release-notes/gimp-2.4.html].
*[http://www.gimp.org/release-notes/gimp-2.4.html http://www.gimp.org/release-notes/gimp-2.4.html].
*[http://www.gimp.org/release-notes/gimp-2.4-videos.html http://www.gimp.org/release-notes/gimp-2.4-videos.html].
*[http://www.gimp.org/release-notes/gimp-2.4-videos.html http://www.gimp.org/release-notes/gimp-2.4-videos.html].
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**Over-sharpening makes images look like caricatures.  
**Over-sharpening makes images look like caricatures.  
*Sharpening should be the last step in post-processing.
*Sharpening should be the last step in post-processing.
==Animation==
[[Image:Squamous carcinoma - lung FNA -- high and very high mag - animation.gif|thumb|right|An animated GIF showing [[squamous carcinoma of the lung]]. (WC)]]
*GIMP has a [https://www.gimp.org/tutorials/Simple_Animations/ nice tutorial (gimp.org)] on how it can be done. 
*Animations are particularly useful for [[cytopathology]].


=See also=
=See also=
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*[[Digital ISO]].
*[[Digital ISO]].
*[[Micrographs]].
*[[Micrographs]].
*[[Image annotation]].
*[[Micrograph wishlist]].


=References=
=References=
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