
Proceedings Paper
Biological imaging with high dynamic range using compressive imaging techniqueFormat | Member Price | Non-Member Price |
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Paper Abstract
Scenes in real world have dynamic range of radiation that cannot be captured by conventional cameras. High dynamic
range imaging is a technique to capture detail images where, in the field of image, intensity variation is extreme. This
technique is very useful for biological imaging where the samples have very bright and very dark regions and both parts
have useful information. In this article we propose a novel high dynamic range imaging technique based on compressive
imaging that uses one single detector instead of camera (array of detectors) to capture an image. Combination of high
dynamic range imaging and compressive imaging benefits from imaging with high dynamic range of radiation and
advantages of compressive sampling; namely, imaging at regions of optical spectrum where conventional cameras are
not readily available and single detectors are available. Additionally, as its name suggests, this technique requires less
number of samples (compared to raster scanning). Our experimental results show that high dynamic range compressive
imaging system is capable of capturing images with large intensity contrast.
Paper Details
Date Published: 9 February 2012
PDF: 7 pages
Proc. SPIE 8225, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X, 82251X (9 February 2012); doi: 10.1117/12.907365
Published in SPIE Proceedings Vol. 8225:
Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X
Daniel L. Farkas; Dan V. Nicolau; Robert C. Leif, Editor(s)
PDF: 7 pages
Proc. SPIE 8225, Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X, 82251X (9 February 2012); doi: 10.1117/12.907365
Show Author Affiliations
Mehrdad Abolbashari, The Univ. of North Carolina at Charlotte (United States)
Gelareh Babaie, The Univ. of North Carolina at Charlotte (United States)
Filipe Magalhães, INESC Porto (Portugal)
Univ. do Porto (Portugal)
Miguel V. Correia, INESC Porto (Portugal)
Univ. do Porto (Portugal)
Gelareh Babaie, The Univ. of North Carolina at Charlotte (United States)
Filipe Magalhães, INESC Porto (Portugal)
Univ. do Porto (Portugal)
Miguel V. Correia, INESC Porto (Portugal)
Univ. do Porto (Portugal)
Francisco M. Araújo, Univ. do Porto (Portugal)
Awad S. Gerges, The Univ. of North Carolina at Charlotte (United States)
Faramarz Farahi, The Univ. of North Carolina at Charlotte (United States)
Awad S. Gerges, The Univ. of North Carolina at Charlotte (United States)
Faramarz Farahi, The Univ. of North Carolina at Charlotte (United States)
Published in SPIE Proceedings Vol. 8225:
Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues X
Daniel L. Farkas; Dan V. Nicolau; Robert C. Leif, Editor(s)
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