Abstract — The validation of image analysis methods used in automated image cytometry has become an important topic. Im-age generation from biological experiments could not guarantee us obtain a complete set of test cases for validation purpose while the ground truth obtained from manual inspection for these images is often questioned for human bias. Also, working on hundreds of thousands of images by hand is impractical. In this paper we propose a computational framework for generating synthesized confocal microscopy images with F-actin structures stained and highlighted by Green Fluorescent Protein (GFP). The presented simulation software was developed in Matlab. It was built primarily to validate our F-actin quantification software devel...
Hardware automation and software development have allowed a dramatic increase of throughput in both ...
Digital image processing and epi-fluorescence microscopy provide one of the main and basic tools for...
Background Manual assessment and evaluation of fluorescent micrograph cell experiments is time-co...
The distribution, directionality and motility of the actin fibers control cell shape, affect cell fu...
The distribution, directionality and motility of the actin fibers control cell shape, affect cell fu...
In recent years many automated methods for detection and tracking of sub cellular structures in live...
The paper reports on a novel method for reconstruction of cellular features including cell nuclei an...
MOTIVATION: Actin filaments are dynamic structures that substantially change their organization over...
ABSTRACT Fluorescent speckle microscopy (FSM) is a new imaging technique with the potential for simu...
ABSTRACTFluorescent speckle microscopy (FSM) is a new imaging technique with the potential for simul...
Abstract—Quantitative confocal microscopy is a powerful analytical tool used to visualize the associ...
Manual evaluation of fluorescent microscopy cell experiments is time-consuming and tedious work. The...
Advances in microscopy automation and image analysis have given biologists the tools to attempt larg...
Since their invention, confocal microscopy and super-resolution microscopy have become important cho...
<p><b>A)</b> Representative immunofluorescence confocal microscopic images of the F-actin (red) of c...
Hardware automation and software development have allowed a dramatic increase of throughput in both ...
Digital image processing and epi-fluorescence microscopy provide one of the main and basic tools for...
Background Manual assessment and evaluation of fluorescent micrograph cell experiments is time-co...
The distribution, directionality and motility of the actin fibers control cell shape, affect cell fu...
The distribution, directionality and motility of the actin fibers control cell shape, affect cell fu...
In recent years many automated methods for detection and tracking of sub cellular structures in live...
The paper reports on a novel method for reconstruction of cellular features including cell nuclei an...
MOTIVATION: Actin filaments are dynamic structures that substantially change their organization over...
ABSTRACT Fluorescent speckle microscopy (FSM) is a new imaging technique with the potential for simu...
ABSTRACTFluorescent speckle microscopy (FSM) is a new imaging technique with the potential for simul...
Abstract—Quantitative confocal microscopy is a powerful analytical tool used to visualize the associ...
Manual evaluation of fluorescent microscopy cell experiments is time-consuming and tedious work. The...
Advances in microscopy automation and image analysis have given biologists the tools to attempt larg...
Since their invention, confocal microscopy and super-resolution microscopy have become important cho...
<p><b>A)</b> Representative immunofluorescence confocal microscopic images of the F-actin (red) of c...
Hardware automation and software development have allowed a dramatic increase of throughput in both ...
Digital image processing and epi-fluorescence microscopy provide one of the main and basic tools for...
Background Manual assessment and evaluation of fluorescent micrograph cell experiments is time-co...