CNN-based two-stage cell segmentation improves plant cell tracking

2019 ◽  
Vol 128 ◽  
pp. 311-317 ◽  
Author(s):  
Wenbo Jiang ◽  
Lehui Wu ◽  
Shihui Liu ◽  
Min Liu
PLoS ONE ◽  
2020 ◽  
Vol 15 (12) ◽  
pp. e0243219
Author(s):  
Tim Scherr ◽  
Katharina Löffler ◽  
Moritz Böhland ◽  
Ralf Mikut

The accurate segmentation and tracking of cells in microscopy image sequences is an important task in biomedical research, e.g., for studying the development of tissues, organs or entire organisms. However, the segmentation of touching cells in images with a low signal-to-noise-ratio is still a challenging problem. In this paper, we present a method for the segmentation of touching cells in microscopy images. By using a novel representation of cell borders, inspired by distance maps, our method is capable to utilize not only touching cells but also close cells in the training process. Furthermore, this representation is notably robust to annotation errors and shows promising results for the segmentation of microscopy images containing in the training data underrepresented or not included cell types. For the prediction of the proposed neighbor distances, an adapted U-Net convolutional neural network (CNN) with two decoder paths is used. In addition, we adapt a graph-based cell tracking algorithm to evaluate our proposed method on the task of cell tracking. The adapted tracking algorithm includes a movement estimation in the cost function to re-link tracks with missing segmentation masks over a short sequence of frames. Our combined tracking by detection method has proven its potential in the IEEE ISBI 2020 Cell Tracking Challenge (http://celltrackingchallenge.net/) where we achieved as team KIT-Sch-GE multiple top three rankings including two top performances using a single segmentation model for the diverse data sets.


2016 ◽  
Vol 208 ◽  
pp. 309-314 ◽  
Author(s):  
Min Liu ◽  
Peng Xiang ◽  
Guocai Liu

2020 ◽  
Author(s):  
JA Solís-Lemus ◽  
BJ Sánchez-Sánchez ◽  
S Marcotti ◽  
M Burki ◽  
B Stramer ◽  
...  

AbstractThis paper compares the contact-repulsion movement of mutant and wild-type macrophages using a novel interaction detection mechanism. The migrating macrophages are observed in Drosophila embryos. The study is carried out by a framework called macrosight, which analyses the movement and interaction of migrating macrophages. The framework incorporates a segmentation and tracking algorithm into analysing motion characteristics of cells after contact. In this particular study, the interactions between cells is characterised in the case of control embryos and Shot3 mutants, where the cells have been altered to suppress a specific protein, looking to understand what drives the movement. Statistical significance between control and mutant cells was found when comparing the direction of motion after contact in specific conditions. Such discoveries provide insights for future developments in combining biological experiments to computational analysis. Cell Segmentation, Cell Tracking, Macrophages, Cell Shape, Contact Analysis


2017 ◽  
Vol 24 (8) ◽  
pp. 1168-1172 ◽  
Author(s):  
Min Liu ◽  
Yangliu Wei ◽  
Weili Qian ◽  
Hongzhong Zhang

2021 ◽  
Author(s):  
Katharina Löffler ◽  
Tim Scherr ◽  
Ralf Mikut

AbstractAutomatic cell segmentation and tracking enables to gain quantitative insights into the processes driving cell migration. To investigate new data with minimal manual effort, cell tracking algorithms should be easy to apply and reduce manual curation time by providing automatic correction of segmentation errors. Current cell tracking algorithms, however, are either easy to apply to new data sets but lack automatic segmentation error correction, or have a vast set of parameters that needs either manual tuning or annotated data for parameter tuning. In this work, we propose a tracking algorithm with only few manually tunable parameters and automatic segmentation error correction. Moreover, no training data is needed. We investigate the performance of our approach by simulating erroneous segmentation data, including false negatives, over- and under-segmentation errors, on 2D and 3D cell data sets. We compare our approach against three well-performing tracking algorithms from the Cell Tracking Challenge. Our tracking algorithm can correct false negatives, over- and under-segmentation errors as well as a mixture of the aforementioned segmentation errors. Furthermore, in case of under-segmentation or a combination of segmentation errors our approach outperforms the other tracking approaches.


PLoS ONE ◽  
2021 ◽  
Vol 16 (9) ◽  
pp. e0249257
Author(s):  
Katharina Löffler ◽  
Tim Scherr ◽  
Ralf Mikut

Automatic cell segmentation and tracking enables to gain quantitative insights into the processes driving cell migration. To investigate new data with minimal manual effort, cell tracking algorithms should be easy to apply and reduce manual curation time by providing automatic correction of segmentation errors. Current cell tracking algorithms, however, are either easy to apply to new data sets but lack automatic segmentation error correction, or have a vast set of parameters that needs either manual tuning or annotated data for parameter tuning. In this work, we propose a tracking algorithm with only few manually tunable parameters and automatic segmentation error correction. Moreover, no training data is needed. We compare the performance of our approach to three well-performing tracking algorithms from the Cell Tracking Challenge on data sets with simulated, degraded segmentation—including false negatives, over- and under-segmentation errors. Our tracking algorithm can correct false negatives, over- and under-segmentation errors as well as a mixture of the aforementioned segmentation errors. On data sets with under-segmentation errors or a mixture of segmentation errors our approach performs best. Moreover, without requiring additional manual tuning, our approach ranks several times in the top 3 on the 6th edition of the Cell Tracking Challenge.


2019 ◽  
Author(s):  
Hsieh-Fu Tsai ◽  
Joanna Gajda ◽  
Tyler F.W. Sloan ◽  
Andrei Rares ◽  
Amy Q. Shen

AbstractStain-free, single-cell segmentation and tracking is tantamount to the holy grail of microscopic cell migration analysis. Phase contrast microscopy (PCM) images with cells at high density are notoriously difficult to segment accurately; thus, manual segmentation remains the de facto standard practice. In this work, we introduce Usiigaci, an all-in-one, semi-automated pipeline to segment, track, and visualize cell movement and morphological changes in PCM. Stain-free, instance-aware segmentation is accomplished using a mask regional convolutional neural network (Mask R-CNN). A Trackpy-based cell tracker with a graphical user interface is developed for cell tracking and data verification. The performance of Usiigaci is validated with electrotaxis of NIH/3T3 fibroblasts. Usiigaci provides highly accurate cell movement and morphological information for quantitative cell migration analysis.


2017 ◽  
Vol 60 ◽  
pp. 154-161 ◽  
Author(s):  
Min Liu ◽  
Yue He ◽  
Yangliu Wei ◽  
Peng Xiang

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