Cell tracking in low-frame-rate video based on displacement prediction
Cell tracking in low-frame-rate video based on displacement prediction
批准号:
10648570
负责人:
Federico Iuricich
金额:
$20.41万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-01 至 2025-08-31
关键词:
A549AddressAffectAirAlgorithmsAreaBiochemistryBioinformaticsBiologicalBiologyCell NucleusCellsCellular biologyCessation of lifeClassificationCloverConsumptionDataData SetDevelopmental BiologyDropsEnvironmentEquipmentEvaluationEventFormulationFutureGeneticHL60HealthHourImageLearningLinkLocomotionMCF10A cellsMDA MB 231Machine LearningMammalian CellManualsMeasuresMedicineMembraneMethodsMicroscopeMorphologic artifactsMorphologyMovementPerformancePhotobleachingPhototoxicityPreparationRegenerative MedicineResearchResearch PersonnelResourcesScienceSpeedTechniquesTemperatureTestingTimeTrainingVisualizationWorkcell analyzercell motilitycell typecellular imagingcostcytatecytotoxicitydeep learningdeep neural networkdesigndrug discoveryimprovedinnovationinterestlight transmissionlive cell imagingneural networknovel strategiesrecurrent neural networktool
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英文摘要
Project Summary
Tracking living cells in video sequences is a fundamental task in many fields of science,
including biochemistry, bioinformatics, cell biology, and genetics. Manually linking cells is
extremely time-consuming and not feasible in large-scale analysis. Automatic approaches can
compute cell links by measuring how close two instances of a cell are, or how similar they look.
These techniques work well with video acquired at a relatively high frame rate, but,
unfortunately, acquiring images at high frame rates affects cells negatively. Too frequent
imaging not only causes phototoxicity, leading to experimental artifacts, but also
photobleaching, leading to the inability to measure quantities of interest over time. In addition,
during image acquisition, the environment temperature and air quality are typically less
controlled, which could also contribute to cytotoxicity. Moreover, when performing high-
throughput live-cell imaging, the lower the acquisition rate, the more cells/plates can be imaged,
and, consequently, the more experimental treatments can be applied and studied.
If reducing the acquisition rate is beneficial for all these reasons, it severely affects the accuracy
of cell tracking algorithms. To this end, we propose a new class of cell tracking approaches based
on cell movement predictions. Instead of comparing cells based on their similarity, we propose
to predict where every cell will move in the next frame. This will allow for searching the
occurrence of such cells, even if the next frame was acquired after an extended period. The
new approach will be investigated using a newly generated dataset for low frame rate cell
tracking (Aim 1). Cell displacement will be predicted by using a new Recurrent Neural Network
designed for the task (Aim 2). Cell tracking algorithms will be defined re-evaluating existing
approaches under low-frame rate constraints when using cell displacement information (Aim
3).
While current approaches require image acquisition to occur at least every 5-15 minutes, we
will investigate the feasibility of cell tracking on images acquired at intervals of up to 2 hours. If
successful, our research will allow to accurately track cells in low frame rate video sequences
without the need for specialized tools or equipment.
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