Time-lapse fluorescence microscopy is a valuable technology in cell biology, but it suffers from the inherent problem of intensity inhomogeneity due to uneven illumination or camera nonlinearity, known as shading artefacts. This will lead to inaccurate estimates of single-cell features such as average and total intensity. Numerous shading correction methods have been proposed to remove this effect. In order to compare the performance of different methods, many quantitative performance measures have been developed. However, there is little discussion about which performance measure should be generally applied for evaluation on real data, where the ground truth is absent. In this paper, the state-of-the-art shading correction methods and perf...
none4noWe propose a novel acquisition scheme and non-parametric multi-image based method for correct...
Abstract- Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, tot...
Quantitative analysis of bioimaging data is often skewed by both shading in space and background var...
Due to the inherent imperfections in the optical path, microscopy images, particularly fluorescence ...
Due to the inherent imperfections in the imaging process, fluorescence microscopy images often suffe...
A comparison of the accuracy and robustness of differ-ent data driven methods for intensity nonunifo...
An image processing system with applications in bacterial (immuno-)fluorescence measurement has been...
In the last few years, single-cell time-lapse fluorescence microscopy has emerged as a key technolog...
A fluorescence image calibration method is presented based on the use of standardized uniformly fluo...
Quantitative imaging and image de-convolution have become standard techniques for the modern cell bi...
A fluorescence image calibration method is introduced based on the use of standardized uniformly flu...
Quantitative analysis of biological image data generally involves the detection of many subresolutio...
Images acquired using optical microscopes are inherently subject to vignetting effects due to imperf...
Quantitative analysis of bioimaging data is often skewed by both shading in space and background var...
There is currently no widely adopted standard for the optical characterisation of fluorescence micro...
none4noWe propose a novel acquisition scheme and non-parametric multi-image based method for correct...
Abstract- Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, tot...
Quantitative analysis of bioimaging data is often skewed by both shading in space and background var...
Due to the inherent imperfections in the optical path, microscopy images, particularly fluorescence ...
Due to the inherent imperfections in the imaging process, fluorescence microscopy images often suffe...
A comparison of the accuracy and robustness of differ-ent data driven methods for intensity nonunifo...
An image processing system with applications in bacterial (immuno-)fluorescence measurement has been...
In the last few years, single-cell time-lapse fluorescence microscopy has emerged as a key technolog...
A fluorescence image calibration method is presented based on the use of standardized uniformly fluo...
Quantitative imaging and image de-convolution have become standard techniques for the modern cell bi...
A fluorescence image calibration method is introduced based on the use of standardized uniformly flu...
Quantitative analysis of biological image data generally involves the detection of many subresolutio...
Images acquired using optical microscopes are inherently subject to vignetting effects due to imperf...
Quantitative analysis of bioimaging data is often skewed by both shading in space and background var...
There is currently no widely adopted standard for the optical characterisation of fluorescence micro...
none4noWe propose a novel acquisition scheme and non-parametric multi-image based method for correct...
Abstract- Fluorescence microscopy imaging is a constant trade off between signal to noise ratio, tot...
Quantitative analysis of bioimaging data is often skewed by both shading in space and background var...