Phase contrast and differential interference contrast, which are used to capture microscopy images of living cells, contain a few artifacts such as halo and shadow-cast effect. Removing these artifacts from microscopy images facilitates automated microscopy image analysis, such as the cell segmentation that is a critical step in cell tracking systems. We propose a restoration algorithm based on the microscopy imaging model and consider temporal consistency when restoring time-lapse microscopy image sequences. The artifact-free microscopy images are restored by minimizing a regularized quadratic cost function that is adaptable to input image properties. Our method achieves high segmentation accuracy and low computational cost compared to the...
ABSTRACT: The quantitative determination of key adherent cell culture characteristics such as conflu...
The goal of modern microscopy is to acquire high-quality image based data sets. A typical microscopy...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...
Phase contrast, a noninvasive microscopy imaging technique, is widely used to capture time-lapse ima...
Image segmentation is essential for many automated microscopy image analysis systems. Rather than tr...
Phase-contrast microscopy is one of the most common and convenient imaging modalities to observe lon...
Automated microscopy image restoration, especially in Differential Interference Contrast (DIC) imagi...
Time-resolved imaging in microscopy is important for the direct observation of a range of dynamic pr...
AbstractTime-resolved imaging in microscopy is important for the direct observation of a range of dy...
The restoration of microscopy images makes the segmentation and detection of cells easier and more r...
We propose a novel cell segmentation approach by estimating a cell-sensitive camera response functio...
The objective of modern microscopy is to acquire high-quality image based data sets. A typical micro...
In this paper, we propose an image processing method able to detect cells trough in vitro phase-cont...
We propose a novel way of imaging live cells in a Petri dish by the phase contrast microscope. By ta...
Automated image restoration in microscopy, especially in Differential Interference Contrast (DIC) im...
ABSTRACT: The quantitative determination of key adherent cell culture characteristics such as conflu...
The goal of modern microscopy is to acquire high-quality image based data sets. A typical microscopy...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...
Phase contrast, a noninvasive microscopy imaging technique, is widely used to capture time-lapse ima...
Image segmentation is essential for many automated microscopy image analysis systems. Rather than tr...
Phase-contrast microscopy is one of the most common and convenient imaging modalities to observe lon...
Automated microscopy image restoration, especially in Differential Interference Contrast (DIC) imagi...
Time-resolved imaging in microscopy is important for the direct observation of a range of dynamic pr...
AbstractTime-resolved imaging in microscopy is important for the direct observation of a range of dy...
The restoration of microscopy images makes the segmentation and detection of cells easier and more r...
We propose a novel cell segmentation approach by estimating a cell-sensitive camera response functio...
The objective of modern microscopy is to acquire high-quality image based data sets. A typical micro...
In this paper, we propose an image processing method able to detect cells trough in vitro phase-cont...
We propose a novel way of imaging live cells in a Petri dish by the phase contrast microscope. By ta...
Automated image restoration in microscopy, especially in Differential Interference Contrast (DIC) im...
ABSTRACT: The quantitative determination of key adherent cell culture characteristics such as conflu...
The goal of modern microscopy is to acquire high-quality image based data sets. A typical microscopy...
The performance of structured illumination microscopy (SIM) is hampered in many biological applicati...