Non-Gaussian Models for Object Motion Analysis with Time-Lapse Fluorescence Microscopy Images

2021 ◽  
pp. 15-41
Author(s):  
Hanyi Yu ◽  
Sung Bo Yoon ◽  
Robert Kauffman ◽  
Jens Wrammert ◽  
Adam Marcus ◽  
...  
2021 ◽  
Author(s):  
Slo-Li Chu ◽  
Kuniya Abe ◽  
Hideo Yokota ◽  
Ming-Dar Tsai

Abstract Purpose Embryonic stem (ES) cells represent as a cellular resource for basic biological studies and for their uses as medically relevant cells in in vitro studies. Fluorescence microscopy images taken during cell culture are frequently used to manually monitor time-series morphology changes and status transitions of ES cell (ESC) colonies, and to study dynamical pattern formation and heterogeneity distribution within ESC colonies, intrinsic fluctuation and cell-cell cooperativity. Therefore, tracking and furthermore predicting morphology changes and status transitions of ESC colonies is an effective method to monitor culture medium for maintaining ES cells in undifferentiated or early differentiated stage. Methods A P-LSTM (Progressive Long Short-Term Memory) structure is proposed to incorporate some new time-lapse images real-time taken from incubators for a new RNN (Recurrent Neural Networks) training. The P-LSTM can achieve adaptive long- and short- term memories to generate accurate predicted images. On the time-lapse images, entropy and bi-lateral filtering are used to extract the range of every colony to calculate colony morphology. Colony status transitions between consecutive images are calculated by mapping the calculated colony centers and ranges. Results Accuracies for the colony status transition, area and roundness for the 15 predicted (five-hour) future frames calculated from 1500-2500 colonies for respective frames show the effectiveness of the proposed method.Conclusion We proposed an efficient and automatic method to predict and monitor status transitions and morphology changes of mouse ESC colonies in culture using time-lapse fluorescence microscopy images.


2010 ◽  
Vol 26 (19) ◽  
pp. 2424-2430 ◽  
Author(s):  
O. Dzyubachyk ◽  
J. Essers ◽  
W. A. v. Cappellen ◽  
C. Baldeyron ◽  
A. Inagaki ◽  
...  

2017 ◽  
Vol 37 (1) ◽  
pp. 18-25 ◽  
Author(s):  
Yuan-Hsiang Chang ◽  
Hideo Yokota ◽  
Kuniya Abe ◽  
Chia-Tong Tang ◽  
Ming-Dar Tasi

2014 ◽  
Vol 2014 ◽  
pp. 1-6
Author(s):  
Liang Yuan ◽  
Junda Zhu

Neurofilament is an important type of intercellular cargos transmitted in neural axons. Given fluorescence microscopy images, existing methods extract neurofilament movement patterns by manual tracking. In this paper, we describe two automated tracking methods for analyzing neurofilament movement based on two different techniques: constrained particle filtering and tracking-by-detection. First, we introduce the constrained particle filtering approach. In this approach, the orientation and position of a particle are constrained by the axon’s shape such that fewer particles are necessary for tracking neurofilament movement than object tracking techniques based on generic particle filtering. Secondly, a tracking-by-detection approach to neurofilament tracking is presented. For this approach, the axon is decomposed into blocks, and the blocks encompassing the moving neurofilaments are detected by graph labeling using Markov random field. Finally, we compare two tracking methods by performing tracking experiments on real time-lapse image sequences of neurofilament movement, and the experimental results show that both methods demonstrate good performance in comparison with the existing approaches, and the tracking accuracy of the tracing-by-detection approach is slightly better between the two.


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