One of the fundamental problems in the analysis of single particle tracking data is the detection of individual particle positions from microscopy images. Distinguishing true particles from noise with a minimum of false positives and false negatives is an important step that will have substantial impact on all further analysis of the data. A common approach is to obtain a plausible set of particles from a larger set of candidate particles by filtering using manually selected threshold values for intensity, size, shape, and other parameters describing a particle. This introduces subjectivity into the analysis and hinders reproducibility. In this paper, we introduce a method for automatic selection of these threshold values based on maximizin...
We propose an object detection method using particle filters. Our approach estimates the probability...
We present a new, robust, computational procedure for tracking fluorescent markers in time-lapse mic...
Particle tracking is of key importance for quantitative analysis of intracellular dynamic processes ...
Quantitative analysis of dynamic processes in living cells by means of fluorescence microscopy imagi...
The aim of this thesis is stochastic modeling and statistical inference in single particle fluoresce...
As new genome sequencing initiatives are completed, one of the next great challenges of cell biology...
The topic of this thesis is the introduction of two novel methods for using single particle microsco...
Automated analysis of fluorescence microscopy data relies on robust segmentation and tracking algori...
Quantitative analysis of dynamical processes in living cells by means of fluorescence microscopy ima...
Two methods of correlation‐based automatic particle detection in electron microscopy images are comp...
Introduction Studying motility of biological objects is an important parameter in many biomedical pr...
An automatic particle picking algorithm for processing electron micrographs of a large molecular com...
Recent advances in optical microscopy have enabled the acquisition of very large datasets from livin...
Analysing migrating cells in microscopy time-lapse images has already helped the understanding of ma...
Quantitative analysis of microscopy images is ideally suited for understanding the functional biolog...
We propose an object detection method using particle filters. Our approach estimates the probability...
We present a new, robust, computational procedure for tracking fluorescent markers in time-lapse mic...
Particle tracking is of key importance for quantitative analysis of intracellular dynamic processes ...
Quantitative analysis of dynamic processes in living cells by means of fluorescence microscopy imagi...
The aim of this thesis is stochastic modeling and statistical inference in single particle fluoresce...
As new genome sequencing initiatives are completed, one of the next great challenges of cell biology...
The topic of this thesis is the introduction of two novel methods for using single particle microsco...
Automated analysis of fluorescence microscopy data relies on robust segmentation and tracking algori...
Quantitative analysis of dynamical processes in living cells by means of fluorescence microscopy ima...
Two methods of correlation‐based automatic particle detection in electron microscopy images are comp...
Introduction Studying motility of biological objects is an important parameter in many biomedical pr...
An automatic particle picking algorithm for processing electron micrographs of a large molecular com...
Recent advances in optical microscopy have enabled the acquisition of very large datasets from livin...
Analysing migrating cells in microscopy time-lapse images has already helped the understanding of ma...
Quantitative analysis of microscopy images is ideally suited for understanding the functional biolog...
We propose an object detection method using particle filters. Our approach estimates the probability...
We present a new, robust, computational procedure for tracking fluorescent markers in time-lapse mic...
Particle tracking is of key importance for quantitative analysis of intracellular dynamic processes ...