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Re: Nyquist sampling advice for a short talk

Posted by Carina Monico-2 on Nov 11, 2020; 9:53am
URL: http://confocal-microscopy-list.275.s1.nabble.com/Nyquist-sampling-advice-for-a-short-talk-tp7591495p7591505.html

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Hi,

I really like the way Jeff Lichtman addresses sampling in his lecture of Resolution of a microscope on iBiology.
https://www.ibiology.org/talks/resolution-of-a-microscope/

Best wishes,

Carina

> On 11 Nov 2020, at 09:30, Straatman, Kees (Dr.) <[hidden email]> wrote:
>
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> But does this not assume that your objects is in de squares. What if the objects are in between two squares? Dividing by 2 would just result in 4 squares with more or less the same intensity. So, I normally advice to divide by 3.
>
> Best wishes
>
> Kees
>
>
> Dr Ir K.R. Straatman
> Advanced Imaging Facility
>
> University of Leicester
> www.le.ac.uk/advanced-imaging-facility<https://eur03.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.le.ac.uk%2Fadvanced-imaging-facility&data=04%7C01%7Ckrs5%40leicester.ac.uk%7C1f8acf823a4542b86f7608d884c0d61a%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637405311048443604%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=9z7hCaL8bVmBGOw0zWZWwcTqbLtWd4foqIM%2FeDFuyUY%3D&reserved=0>
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> ________________________________
> From: Confocal Microscopy List <[hidden email]> on behalf of Benjamin Smith <[hidden email]>
> Sent: 10 November 2020 16:42
> To: [hidden email] <[hidden email]>
> Subject: Re: Nyquist sampling advice for a short talk
>
> *****
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> GIven that most microscopy has the luxury of being a simpler specific case
> of the Nyquist sampling theorem, I like to simplify it to a discrete model
> using a checkerboard.  I first show a grid of squares and ask, "What is the
> smallest feature we can resolve on this grid?"  I then show a checkerboard
> pattern next to a grid with all white squares.  I point out that in order
> to resolve two objects means to be able to distinguish between two point
> sources and one bigger solid source.  Therefore, you need to sample not
> only the peak intensities (your resolution) but also a local minimum
> between them to distinguish a pair of points from a solid object.
> Therefore, you need to sample at 2x your resolution.
>
> The hope here is to give people an intuitive sense of where Nyquist
> sampling theory comes from without delving into more complex issues like
> aliasing.
>
> On Tue, Nov 10, 2020 at 8:26 AM Sara Parker <[hidden email]>
> wrote:
>
>> *****
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>>
>> Dale,
>>
>> I really like the following applets for demonstrating resolution and
>> sampling in practice, and connecting theory to experimental design.
>>
>> https://eur03.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.iscopecalc.com%2F&amp;data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134631398%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&amp;sdata=ure5inAP00fuI4A6vWsRdgvpskjbhqQWrTnNPOGTrhg%3D&amp;reserved=0
>>
>> https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olympus-lifescience.com%2Fen%2Fmicroscope-resource%2Fprimer%2Fjava%2Fimageformation%2Frayleighdisks%2F&amp;data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134641396%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&amp;sdata=E90C0TWKjpw2mx5UNXRlI5VtvxmNcq8n1yftIDmU%2BO0%3D&amp;reserved=0
>>
>> Sara Parker
>> Postdoctoral Fellow, Mouneimne Lab
>> (520) 626-3860
>> [hidden email]
>> Department of Cellular & Molecular Medicine
>> University of Arizona
>>
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