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1.
IEEE J Biomed Health Inform ; 28(7): 4157-4169, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38662560

ABSTRACT

Multi-Object tracking in real world environments is a tough problem, especially for cell morphogenesis with division. Most cell tracking methods are hard to achieve reliable mitosis detection, efficient inter-frame matching, and accurate state estimation simultaneously within a unified tracking framework. In this paper, we propose a novel unified framework that leverages a spatio-temporal ant colony evolutionary algorithm to track cells amidst mitosis under measurement uncertainty. Each Bernoulli ant colony representing a migrating cell is able to capture the occurrence of mitosis through the proposed Isolation Random Forest (IRF)-assisted temporal mitosis detection algorithm with the assumption that mitotic cells exhibit unique spatio-temporal features different from non-mitotic ones. Guided by prediction of a division event, multiple ant colonies evolve between consecutive frames according to an augmented assignment matrix solved by the extended Hungarian method. To handle dense cell populations, an efficient group partition between cells and measurements is exploited, which enables multiple assignment tasks to be executed in parallel with a reduction in matrix dimension. After inter-frame traversing, the ant colony transitions to a foraging stage in which it begins approximating the Bernoulli parameter to estimate cell state by iteratively updating its pheromone field. Experiments on multi-cell tracking in the presence of cell mitosis and morphological changes are conducted, and the results demonstrate that the proposed method outperforms state-of-the-art approaches, striking a balance between accuracy and computational efficiency.


Subject(s)
Algorithms , Cell Tracking , Time-Lapse Imaging , Cell Tracking/methods , Time-Lapse Imaging/methods , Animals , Mitosis/physiology , Humans , Image Processing, Computer-Assisted/methods , Ants/physiology , Ants/cytology , Random Forest
2.
IEEE/ACM Trans Comput Biol Bioinform ; 18(5): 1850-1863, 2021.
Article in English | MEDLINE | ID: mdl-31751247

ABSTRACT

In this article, we take as inspiration the labor division into scouts and workers in an ant colony and propose a novel approach for automated cell tracking in the framework of multi-Bernoulli random finite sets. To approximate the Bernoulli parameter sets, we first define an existence probability of an ant colony as well as its discrete density distribution. During foraging, the behavior of scouts is modeled as a chaotic movement to produce a set of potential candidates. Afterwards, a group of workers, i.e., a worker ant colony, is recruited for each candidate, which then embark on gathering heuristic information in a self-organized way. Finally, the pheromone field is formed by the corresponding worker ant colony, from which the Bernoulli parameter is derived and the state of the cell is estimated accordingly to be associated with the existing tracks. Performance comparisons with other previous approaches are conducted on both simulated and real cell image sequences and show the superiority of this algorithm.


Subject(s)
Cell Tracking/methods , Computational Biology/methods , Models, Biological , Algorithms , Animals , Ants , Bayes Theorem , Behavior, Animal , Pheromones
3.
IEEE J Biomed Health Inform ; 25(6): 2338-2349, 2021 06.
Article in English | MEDLINE | ID: mdl-33079687

ABSTRACT

In this paper, we use an ant colony heuristic method to tackle the integration of data association and state estimation in the presence of cell mitosis, morphological change and uncertainty of measurement. Our approach first models the scouting behavior of an unlabeled ant colony as a chaotic process to generate a set of cell candidates in the current frame, then a labeled ant colony foraging process is modeled to construct an interframe matching between previously estimated cell states and current cell candidates through minimizing the optimal sub-pattern assignment metric for track (OSPA-T). The states of cells in the current frame are finally estimated using labeled ant colonies via a multi-Bernoulli parameter set approximated by individual food pheromone fields and heuristic information within the same region of support, the resulting trail pheromone fields over frames constitutes the cell lineage trees of the tracks. A four-stage track recovery strategy is proposed to monitor the history of all established tracks to reconstruct broken tracks in a computationally economic way. The labeling method used in this work is an improvement on previous techniques. The method has been evaluated on publicly available, challenging cell image sequences, and a satisfied performance improvement is achieved in contrast to the state-of-the-art methods.


Subject(s)
Algorithms , Pheromones , Cell Cycle
4.
IEEE J Biomed Health Inform ; 24(6): 1703-1716, 2020 06.
Article in English | MEDLINE | ID: mdl-31670688

ABSTRACT

The analysis of the dynamic behavior of cells in time-lapse microscopy sequences requires the development of reliable and automatic tracking methods capable of estimating individual cell states and delineating the lineage trees corresponding to the tracks. In this paper, we propose a novel approach, i.e., an ant colony inspired multi-Bernoulli filter, to handle the tracking of a collection of cells within which mitosis, morphological change and erratic dynamics occur. The proposed technique treats each ant colony as an independent one in an ant society, and the existence probability of an ant colony and its density distribution approximation are derived from the individual pheromone field and the corresponding heuristic information for the approximation to the multi-Bernoulli parameters. To effectively guide ant foraging between consecutive frames, a dual prediction mechanism is proposed for the ant colony and its pheromone field. The algorithm performance is tested on challenging datasets with varying population density, frequent cell mitosis and uneven motion over time, demonstrating that the algorithm outperforms recently reported approaches.


Subject(s)
Algorithms , Cell Tracking/methods , Microscopy/methods , Time-Lapse Imaging/methods , Cell Line , Cell Movement/physiology , Humans , Mitosis/physiology , Models, Biological
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