SHORT TRAJECTORY SEGMENTATION WITH 1D UNET FRAMEWORK: APPLICATION TO SECRETORY VESICLE DYNAMICS

被引:0
|
作者
Dmitrieva, Manila [1 ]
Lefebvre, Joel [1 ]
Penas, Kristofer delas [1 ,3 ]
Zenner, Helen L. [2 ]
Richens, Jennifer [2 ]
St Johnston, Daniel [2 ]
Rittscher, Jens [1 ]
机构
[1] Univ Oxford, Dept Engn Sci, Oxford, England
[2] Univ Cambridge, Gurdon Inst, Cambridge, England
[3] Univ Philippines, Dept Comp Sci, Quezon City, Philippines
来源
2020 IEEE 17TH INTERNATIONAL SYMPOSIUM ON BIOMEDICAL IMAGING (ISBI 2020) | 2020年
基金
英国惠康基金; 英国工程与自然科学研究理事会; 芬兰科学院;
关键词
protein trafficking; trajectory segmentation; deep learning; U-Net; sliding window;
D O I
10.1109/isbi45749.2020.9098426
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The study of protein transport in living cell requires automated techniques to capture and quantify dynamics of the protein packaged into secretory vesicles. The movement of the vesicles is not consistent along the trajectory, therefore the quantitative study of their dynamics requires trajectories segmentation. This paper explores quantification of such vesicle dynamics and introduces a novel 1D U-Net based trajectory segmentation. Unlike existing mean squared displacement based methods, our proposed framework is not restricted under the requirement of long trajectories for effective segmentation. Moreover, as our approach provides segmentation within each sliding window, it enables effectively capture even short segments. The approach is quantified by the data acquired from spinning disk microscopy imaging of protein trafficking in Drosophila epithelial cells. The extracted trajectories have lengths ranging from 5 (short tracks) to 135 (long tracks) points. The proposed approach achieves 77.7% accuracy for the trajectory segmentation.
引用
收藏
页码:891 / 894
页数:4
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