Publication:
Adaptive tracking algorithm for trajectory analysis of cells and layer-by-layer assessment of motility dynamics

dc.contributor.coauthorBayraktar, Halil
dc.contributor.departmentN/A
dc.contributor.departmentDepartment of Molecular Biology and Genetics
dc.contributor.kuauthorQureshi, Mohammad Haroon
dc.contributor.kuprofilePhD Student
dc.contributor.kuprofileFaculty Member
dc.contributor.otherDepartment of Molecular Biology and Genetics
dc.contributor.researchcenterKoç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM)
dc.contributor.researchcenterN/A
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.contributor.yokidN/A
dc.contributor.yokid105301
dc.date.accessioned2024-11-10T00:00:10Z
dc.date.issued2022
dc.description.abstractTracking biological objects such as cells or subcellular components imaged with time-lapse microscopy enables us to understand the molecular principles about the dynamics of cell behaviors. However, automatic object detection, segmentation and extracting trajectories remain as a rate-limiting step due to intrinsic challenges of video processing. This paper presents an adaptive tracking algorithm (Adtari) that automatically finds the op-timum search radius and cell linkages to determine trajectories in consecutive frames. A critical assumption in most tracking studies is that displacement remains unchanged throughout the movie and cells in a few frames are usually analyzed to determine its magnitude. Tracking errors and inaccurate association of cells may occur if the user does not correctly evaluate the value or prior knowledge is not present on cell movement. The key novelty of our method is that minimum intercellular distance and maximum displacement of cells between frames are dynamically computed and used to determine the threshold distance. Since the space between cells is highly variable in a given frame, our software recursively alters the magnitude to determine all plausible matches in the trajectory analysis. Our method therefore eliminates a major preprocessing step where a constant distance was used to determine the neighbor cells in tracking methods. Cells having multiple overlaps and splitting events were further evaluated by using the shape attributes including perimeter, area, ellipticity and distance. The features were applied to determine the closest matches by minimizing the difference in their magnitudes. Finally, reporting section of our software were used to generate instant maps by overlaying cell features and trajectories. Adtari was validated by using videos with variable signal-to-noise, contrast ratio and cell density. We compared the adaptive tracking with constant distance and other methods to evaluate performance and its efficiency. Our algorithm yields reduced mismatch ratio, increased ratio of whole cell track, higher frame tracking efficiency and allows layer-by-layer assessment of motility to characterize single-cells. Adaptive tracking provides a reliable, accurate, time efficient and user-friendly open source software that is well suited for analysis of 2D fluorescence microscopy video datasets.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsorshipITU-BAP
dc.description.sponsorshipNewton Advanced Fellowship
dc.description.sponsorship[2020-42579] Acknowledgement This work was financially supported by ITU-BAP with grant number 2020-42579 (H.B.) . N.O. acknowledges the financial support from Newton Advanced Fellowship. We thank the members of the Bayraktar laboratory for their helpful discussions. We gratefully acknowledge Prof. Dr. Eva Bartova for allowing us to use video sets deposited at CTC. We also thank the Bioimaging Center at Ko? University for assistance to use of time-lapse fluorescence microscope.
dc.description.volume150
dc.identifier.doi10.1016/j.compbiomed.2022.106193
dc.identifier.eissn1879-0534
dc.identifier.issn0010-4825
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85140291104
dc.identifier.urihttp://dx.doi.org/10.1016/j.compbiomed.2022.106193
dc.identifier.urihttps://hdl.handle.net/20.500.14288/15761
dc.identifier.wos875644300003
dc.keywordsTracking
dc.keywordsSegmentation
dc.keywordsAlgorithms
dc.keywordsImage processing
dc.keywordsCell trajectories
dc.keywordsLinkage analysis
dc.keywordsNetworks
dc.keywordsOpen source software
dc.keywordsMotility dynamics
dc.keywordsSingle cell
dc.keywordsContrast video microscopy
dc.keywordsSingle-particle tracking
dc.keywordsAutomatic segmentation
dc.keywordsIn-vitro
dc.keywordsQuantitative-analysis
dc.keywordsMigrating cells
dc.keywordsLevel sets
dc.keywordsNuclei
dc.keywordsCycle
dc.keywordsTolls
dc.languageEnglish
dc.publisherPergamon-Elsevier Science Ltd
dc.sourceComputers in Biology and Medicine
dc.subjectBiology
dc.subjectComputer science
dc.subjectEngineering
dc.subjectBiomedical engineering
dc.subjectMathematical and computational biology
dc.titleAdaptive tracking algorithm for trajectory analysis of cells and layer-by-layer assessment of motility dynamics
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0002-2376-1246
local.contributor.authorid0000-0002-5157-8780
local.contributor.kuauthorQureshi, Mohammad Haroon
local.contributor.kuauthorÖzlü, Nurhan
relation.isOrgUnitOfPublicationaee2d329-aabe-4b58-ba67-09dbf8575547
relation.isOrgUnitOfPublication.latestForDiscoveryaee2d329-aabe-4b58-ba67-09dbf8575547

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