With a perfectly uniform illumination, the amount and concentration of fluorophores in any (biological) sample can be read directly from fluorescence micrographs. However, non-uniform illumination in optical micrographs is a common, yet avoidable artefact, often caused by the setup of the microscope, or by inherent properties caused by the nature of the sample. In this paper, we demonstrate simple matrix-based methods using the common computing environments MATLAB and Python to correct nonuniform illumination, using either a background image or extracting illumination information directly from the sample image, together with subsequent image processing. We compare the processes, algorithms, and results obtained from both MATLAB (commerciall...
International audienceAutomated acquisitions in microscopy may come along with strong illumination a...
International audienceWe propose a reconstruction algorithm called al-goRIM for super-resolution flu...
International audienceStructured illumination microscopy (SIM) is a powerful technique for obtaining...
With a perfectly uniform illumination, the amount and concentration of fluorophores in any (biologic...
We propose a novel solution to the correction of illumination non-uniformity without removing the im...
A comparison of the accuracy and robustness of differ-ent data driven methods for intensity nonunifo...
Due to the overlapping emission spectra of fluorophores, fluorescence microscopy images often have b...
Due to the inherent imperfections in the imaging process, fluorescence microscopy images often suffe...
Due to the inherent imperfections in the optical path, microscopy images, particularly fluorescence ...
none4noWe propose a novel acquisition scheme and non-parametric multi-image based method for correct...
Thesis: S.M., Massachusetts Institute of Technology, School of Architecture and Planning, Program in...
Single-Molecule Localization Microscopy is a powerful imaging technique which enables the localizati...
Structured illumination microscopy (SIM) is one of the most widely applied super-resolution microsco...
Uneven illumination affects every image acquired by a microscope. It is often overlooked, but it can...
The resolution of an optical microscope is limited to roughly 250 nm for biological imaging. This is...
International audienceAutomated acquisitions in microscopy may come along with strong illumination a...
International audienceWe propose a reconstruction algorithm called al-goRIM for super-resolution flu...
International audienceStructured illumination microscopy (SIM) is a powerful technique for obtaining...
With a perfectly uniform illumination, the amount and concentration of fluorophores in any (biologic...
We propose a novel solution to the correction of illumination non-uniformity without removing the im...
A comparison of the accuracy and robustness of differ-ent data driven methods for intensity nonunifo...
Due to the overlapping emission spectra of fluorophores, fluorescence microscopy images often have b...
Due to the inherent imperfections in the imaging process, fluorescence microscopy images often suffe...
Due to the inherent imperfections in the optical path, microscopy images, particularly fluorescence ...
none4noWe propose a novel acquisition scheme and non-parametric multi-image based method for correct...
Thesis: S.M., Massachusetts Institute of Technology, School of Architecture and Planning, Program in...
Single-Molecule Localization Microscopy is a powerful imaging technique which enables the localizati...
Structured illumination microscopy (SIM) is one of the most widely applied super-resolution microsco...
Uneven illumination affects every image acquired by a microscope. It is often overlooked, but it can...
The resolution of an optical microscope is limited to roughly 250 nm for biological imaging. This is...
International audienceAutomated acquisitions in microscopy may come along with strong illumination a...
International audienceWe propose a reconstruction algorithm called al-goRIM for super-resolution flu...
International audienceStructured illumination microscopy (SIM) is a powerful technique for obtaining...