31 research outputs found
Globally Optimal Cell Tracking using Integer Programming
We propose a novel approach to automatically tracking cell populations in
time-lapse images. To account for cell occlusions and overlaps, we introduce a
robust method that generates an over-complete set of competing detection
hypotheses. We then perform detection and tracking simultaneously on these
hypotheses by solving to optimality an integer program with only one type of
flow variables. This eliminates the need for heuristics to handle missed
detections due to occlusions and complex morphology. We demonstrate the
effectiveness of our approach on a range of challenging sequences consisting of
clumped cells and show that it outperforms state-of-the-art techniques.Comment: Engin T\"uretken and Xinchao Wang contributed equally to this wor
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NucliTrack: An integrated nuclei tracking application
Summary: Live imaging studies give unparalleled insight into dynamic single cell behaviours and fate decisions. However, the challenge of reliably tracking single cells over long periods of time limits both the throughput and ease with which such studies can be performed. Here, we present NucliTrack, a cross platform solution for automatically segmenting, tracking and extracting features from fluorescently-labelled nuclei. NucliTrack performs similarly to other state-of-the-art cell tracking algorithms, but NucliTrack's interactive, graphical interface makes it significantly more user friendly. Availability: NucliTrack is available as a free, cross platform application, and open source Python package. Installation details and documentation are at: http://nuclitrack.readthedocs.io/en/latest / A video guide can be viewed online: https://www.youtube.com/watch?v=J6e0D9F-qSU Source code is available through Github: https://github.com/samocooper/nuclitrack . A Matlab toolbox is also available at: https://uk.mathworks.com/matlabcentral/fileexchange/61479-samocooper-nuclitrack-matlab. Contact: [email protected]. Supplementary information: Supplementary data are available at Bioinformatics online
Cell Segmentation and Tracking using CNN-Based Distance Predictions and a Graph-Based Matching Strategy
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.Comment: 25 pages, 14 figures, methods of the team KIT-Sch-GE for the IEEE
ISBI 2020 Cell Tracking Challeng
Time-resolved imaging-based CRISPRi screening
Our ability to connect genotypic variation to biologically important phenotypes has been seriously limited by the gap between live-cell microscopy and library-scale genomic engineering. Here, we show how in situ genotyping of a library of strains after time-lapse imaging in a microfluidic device overcomes this problem. We determine how 235 different CRISPR interference knockdowns impact the coordination of the replication and division cycles of Escherichia coli by monitoring the location of replication forks throughout on average >500 cell cycles per knockdown. Subsequent in situ genotyping allows us to map each phenotype distribution to a specific genetic perturbation to determine which genes are important for cell cycle control. The single-cell time-resolved assay allows us to determine the distribution of single-cell growth rates, cell division sizes and replication initiation volumes. The technology presented in this study enables genome-scale screens of most live-cell microscopy assays
Accurate cell tracking and lineage construction in live-cell imaging experiments with deep learning
Live-cell imaging experiments have opened an exciting window into the behavior of living systems. While these experiments can produce rich data, the computational analysis of these datasets is challenging. Single-cell analysis requires that cells be accurately identified in each image and subsequently tracked over time. Increasingly, deep learning is being used to interpret microscopy image with single cell resolution. In this work, we apply deep learning to the problem of tracking single cells in live-cell imaging data. Using crowdsourcing and a human-in-the-loop approach to data annotation, we constructed a dataset of over 11,000 trajectories of cell nuclei that includes lineage information. Using this dataset, we successfully trained a deep learning model to perform cell tracking within a linear programming framework. Benchmarking tests demonstrate that our method achieves state-of-the-art performance on the task of cell tracking with respect to multiple accuracy metrics. Further, we show that our deep learning-based method generalizes to perform cell tracking for both fluorescent and brightfield images of the cell cytoplasm, despite having never been trained those data types. This enables analysis of live-cell imaging data collected across imaging modalities. A persistent cloud deployment of our cell tracker is available at http://www.deepcell.org
Detecting and Tracking Cells using Network Flow Programming
We propose a novel approach to automatically detecting and tracking cell populations in time-lapse images. Unlike earlier ones that rely on linking a predetermined and potentially under-complete set of detections, we generate an overcomplete set of competing detection hypotheses. We then perform detection and tracking simultaneously by solving an integer program to find an optimal and consistent subset. This eliminates the need for heuristics to handle missed detections due to occlusions and complex morphology. We demonstrate the effectiveness of our approach on a range of challenging image sequences consisting of clumped cells and show that it outperforms state-of-the-art techniques