In this report, we discuss the interest of quality metrics for imaging and image processing of multi-views in light sheet fluorescent 3D microscopy. Various metrics of focus are tested on real and simulated data so as to automatically assess the informational quality of the images. Application of such metrics are given for several information tasks including online control of acquisition, fast registration or image fusion. Illustrations are given for typical samples of interest for in vivo imaging with light sheet microscopy such as spheroids or organoids. We point to the reader softwares freely available under Fiji which enable to test the computation of a basic quality metric, for registration and fusion
International audienceFluorescence standards allow for quality control and for the comparison of dat...
Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, total observ...
Light sheet microscopy is an emerging technique allowing comprehensive visualization of dynamic biol...
In this report, we discuss the interest of quality metrics for imaging and image processing of multi...
The image quality determining and comparison of digital microscopes is important so that repeatable ...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
Three-dimensional fluorescence imaging is an essential tool in biology, used for everything from lon...
The impact of light-sheet fluorescence microscopy (LSFM) is visible in fields as diverse as developm...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
The depth of focus is a constraint of all the light microscopes, being not possible to acquire a sin...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
Fluorescence microscopy is an essential tool in biomedical sciences that allows specific molecules t...
We propose and demonstrate a limited-view light sheet microscopy (LV-LSM) for three dimensional (3D)...
The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objectiv...
In light sheet microscopy, optical sectioning by selective fluorescence excitation with a sheet of l...
International audienceFluorescence standards allow for quality control and for the comparison of dat...
Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, total observ...
Light sheet microscopy is an emerging technique allowing comprehensive visualization of dynamic biol...
In this report, we discuss the interest of quality metrics for imaging and image processing of multi...
The image quality determining and comparison of digital microscopes is important so that repeatable ...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
Three-dimensional fluorescence imaging is an essential tool in biology, used for everything from lon...
The impact of light-sheet fluorescence microscopy (LSFM) is visible in fields as diverse as developm...
We developed a multiple light-sheet microscopy (MLSM) system capable of 3D fluorescence imaging. Emp...
The depth of focus is a constraint of all the light microscopes, being not possible to acquire a sin...
Due to the classical conflict between spatial and temporal resolution, microscopy studies of fast ev...
Fluorescence microscopy is an essential tool in biomedical sciences that allows specific molecules t...
We propose and demonstrate a limited-view light sheet microscopy (LV-LSM) for three dimensional (3D)...
The conventional optical microscope is an inherently two-dimensional (2D) imaging tool. The objectiv...
In light sheet microscopy, optical sectioning by selective fluorescence excitation with a sheet of l...
International audienceFluorescence standards allow for quality control and for the comparison of dat...
Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, total observ...
Light sheet microscopy is an emerging technique allowing comprehensive visualization of dynamic biol...