Due to the limited depth of field of brightfield microscopes, it is usually impossible to image thick specimens entirely in focus. By optically sectioning the specimen, the in-focus information at the specimen's surface can be acquired over a range of images. Commonly based on a high-pass criterion, extended-depth-of-field methods aim at combining the in-focus information from these images into a single image of the texture on the specimen's surface. The topography provided by such methods is usually limited to a map of selected in-focus pixel positions and is inherently discretized along the axial direction, which limits its use for quantitative evaluation. In this paper, we propose a method that jointly estimates the texture and topograph...
We present a novel approach for deconvolution of 3D image stacks of cortical tissue taken by mosaic/...
The previously developed depth-variant expectation maximization (DVEM) restoration algorithm for flu...
The ultimate aim of fluorescence microscopy is to achieve high-resolution imaging of increasingly la...
A rigorous, new, depth-from-focus algorithm is proposed: microscope images at a series of focal plan...
Cells and tissues have complex 3-D surface topologies intimately related to their extracellular envi...
The sampling patterns of the light field microscope (LFM) are highly depth-dependent, which implies ...
To achieve optimal image quality in bright field microscopy, the slide surface should be perpendicul...
Effectiveness of extended depth of field microscopy (EDFM) implementation with wavefront encoding me...
Three-dimensional reconstruction in brightfield microscopy is challenging since a 2D image includes ...
International audienceThe standard two-dimensional (2D) image recorded in bright-field fluorescence ...
Super-resolution microscopes (such as STED) illuminate samples with a tiny spot, and achieve very hi...
One of the most fundamental concepts of microscopy is that of resolution–the ability to clearly dist...
An inverse relationship exists in optical systems between the depth of field (DOF) and the minimum r...
Super-resolution techniques overcome the diffraction-limit and get very high resolutions. A category...
Abstract: The objective of this study is to investigate the use of deconvolution for improving the t...
We present a novel approach for deconvolution of 3D image stacks of cortical tissue taken by mosaic/...
The previously developed depth-variant expectation maximization (DVEM) restoration algorithm for flu...
The ultimate aim of fluorescence microscopy is to achieve high-resolution imaging of increasingly la...
A rigorous, new, depth-from-focus algorithm is proposed: microscope images at a series of focal plan...
Cells and tissues have complex 3-D surface topologies intimately related to their extracellular envi...
The sampling patterns of the light field microscope (LFM) are highly depth-dependent, which implies ...
To achieve optimal image quality in bright field microscopy, the slide surface should be perpendicul...
Effectiveness of extended depth of field microscopy (EDFM) implementation with wavefront encoding me...
Three-dimensional reconstruction in brightfield microscopy is challenging since a 2D image includes ...
International audienceThe standard two-dimensional (2D) image recorded in bright-field fluorescence ...
Super-resolution microscopes (such as STED) illuminate samples with a tiny spot, and achieve very hi...
One of the most fundamental concepts of microscopy is that of resolution–the ability to clearly dist...
An inverse relationship exists in optical systems between the depth of field (DOF) and the minimum r...
Super-resolution techniques overcome the diffraction-limit and get very high resolutions. A category...
Abstract: The objective of this study is to investigate the use of deconvolution for improving the t...
We present a novel approach for deconvolution of 3D image stacks of cortical tissue taken by mosaic/...
The previously developed depth-variant expectation maximization (DVEM) restoration algorithm for flu...
The ultimate aim of fluorescence microscopy is to achieve high-resolution imaging of increasingly la...