Significance: Machine learning is increasingly being applied to the classification of microscopic data. In order to detect some complex and dynamic cellular processes, time-resolved live-cell imaging might be necessary. Incorporating the temporal information into the classification process may allow for a better and more specific classification. Aim: We propose a methodology for cell classification based on the time-lapse quantitative phase images (QPIs) gained by digital holographic microscopy (DHM) with the goal of increasing performance of classification of dynamic cellular processes. Approach: The methodology was demonstrated by studying epithelial-mesenchymal transition (EMT) which entails major and distinct time-dependent morphologica...
Automated time-lapse microscopy can visualize proliferation of large numbers of individual cells, en...
Background: Automated time-lapse microscopy can visualize proliferation of large numbers of individu...
We present a fully automatic method to track and quantify the morphodynamics of differentiating neur...
In the last few years, classification of cells by machine learning has become frequently used in bio...
International audienceFluorescence time-lapse imaging has become a powerful tool to investigate comp...
Author Posting. © The Authors, 2010. This is the author's version of the work. It is posted here by...
<p>Time-lapse live cell imaging has been increasingly employed by biological and biomedical research...
Cells in complex organisms can transition between epithelial and mesenchymal phenotypes during both ...
Advances in fluorescent probing and microscopic imaging technology provide important tools for biolo...
Quantitative phase microscopy (QPM) enables studies of living biological systems without exogenous l...
This book introduces time-stretch quantitative phase imaging (TS-QPI), a high-throughput label-free ...
With the proliferation of modern microscopy imaging technologies the amount of data that has to be a...
Studies of drug effects on cancer cells are performed through measuring cell cycle progression such ...
Recent development of in vivo microscopy techniques, including green fluorescent proteins, has allow...
Holographic cytometry (HC) has been developed as an ultra-high throughput implementation of quantita...
Automated time-lapse microscopy can visualize proliferation of large numbers of individual cells, en...
Background: Automated time-lapse microscopy can visualize proliferation of large numbers of individu...
We present a fully automatic method to track and quantify the morphodynamics of differentiating neur...
In the last few years, classification of cells by machine learning has become frequently used in bio...
International audienceFluorescence time-lapse imaging has become a powerful tool to investigate comp...
Author Posting. © The Authors, 2010. This is the author's version of the work. It is posted here by...
<p>Time-lapse live cell imaging has been increasingly employed by biological and biomedical research...
Cells in complex organisms can transition between epithelial and mesenchymal phenotypes during both ...
Advances in fluorescent probing and microscopic imaging technology provide important tools for biolo...
Quantitative phase microscopy (QPM) enables studies of living biological systems without exogenous l...
This book introduces time-stretch quantitative phase imaging (TS-QPI), a high-throughput label-free ...
With the proliferation of modern microscopy imaging technologies the amount of data that has to be a...
Studies of drug effects on cancer cells are performed through measuring cell cycle progression such ...
Recent development of in vivo microscopy techniques, including green fluorescent proteins, has allow...
Holographic cytometry (HC) has been developed as an ultra-high throughput implementation of quantita...
Automated time-lapse microscopy can visualize proliferation of large numbers of individual cells, en...
Background: Automated time-lapse microscopy can visualize proliferation of large numbers of individu...
We present a fully automatic method to track and quantify the morphodynamics of differentiating neur...