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Article
English
2006

Light field microscopy

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English
2006
DOI: 10.1145/1179352.1141976

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Mark Horowitz
Mark Horowitz

Stanford University

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Marc Levoy
Ren Ng
Andrew Adams
+2 more

Abstract

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.

How to cite this publication

Marc Levoy, Ren Ng, Andrew Adams, Matthew J. Footer, Mark Horowitz (2006). Light field microscopy. , DOI: 10.1145/1179352.1141976.

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Publication Details

Type

Article

Year

2006

Authors

5

Datasets

0

Total Files

0

Language

English

DOI

10.1145/1179352.1141976

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