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Light field microscopy
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- Marc Levoy
- Stanford University
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- Ren Ng
- Stanford University
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- Matthew Footer
- Stanford University
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- Mark Horowitz
- Stanford University
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- Andrew Adams
- Stanford University
Bibliographic Information
- Published
- 2006-07
- Rights Information
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- https://www.acm.org/publications/policies/copyright_policy#Background
- DOI
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- 10.1145/1141911.1141976
- Publisher
- Association for Computing Machinery (ACM)
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Description
<jats:p>By inserting a microlens array into the optical train of a conventional microscope, one can capture light fields of biological specimens in a single photograph. Although diffraction places a limit on the product of spatial and angular resolution in these light fields, we can nevertheless produce useful perspective views and focal stacks from them. Since microscopes are inherently orthographic devices, perspective views represent a new way to look at microscopic specimens. The ability to create focal stacks from a single photograph allows moving or light-sensitive specimens to be recorded. Applying 3D deconvolution to these focal stacks, we can produce a set of cross sections, which can be visualized using volume rendering. In this paper, we demonstrate a prototype light field microscope (LFM), analyze its optical performance, and show perspective views, focal stacks, and reconstructed volumes for a variety of biological specimens. We also show that synthetic focusing followed by 3D deconvolution is equivalent to applying limited-angle tomography directly to the 4D light field.</jats:p>
Journal
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- ACM Transactions on Graphics
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ACM Transactions on Graphics 25 (3), 924-934, 2006-07
Association for Computing Machinery (ACM)
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Details 詳細情報について
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- CRID
- 1361981471044545536
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- ISSN
- 15577368
- 07300301
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- Data Source
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- Crossref

