Treffer: Cell Tracking in 3D using deep learning segmentations

Title:
Cell Tracking in 3D using deep learning segmentations
Contributors:
Génétique et Biologie du Développement, Institut Curie [Paris]-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)
Source:
Python in Science Conference. :154-161
Publisher Information:
CCSD, 2021.
Publication Year:
2021
Collection:
collection:INSERM
collection:CNRS
collection:FNCLCC
collection:CURIE
collection:UGBDD
collection:PSL
collection:SORBONNE-UNIVERSITE
collection:SORBONNE-UNIV
collection:SU-MEDECINE
collection:SU-SCIENCES
collection:SU-MED
collection:TEST-HALCNRS
collection:INSTITUT-CURIE-PSL
collection:SU-TI
collection:ALLIANCE-SU
collection:TEST3-HALCNRS
collection:SUPRA_BIOLOGIE
Subject Geographic:
Original Identifier:
HAL: hal-03329721
Document Type:
Konferenz conferenceObject<br />Conference papers
Language:
English
Relation:
info:eu-repo/semantics/altIdentifier/doi/10.25080/majora-1b6fd038-02b
DOI:
10.25080/majora-1b6fd038-02b
Rights:
info:eu-repo/semantics/OpenAccess
Accession Number:
edshal.hal.03329721v1
Database:
HAL

Weitere Informationen

Live-cell imaging is a highly used technique to study cell migration and dynamics over time. Although many computational tools have been developed during the past years to automatically detect and track cells, they are optimized to detect cell nuclei with similar shapes and/or cells not clustering together. These existing tools are challenged when tracking fluorescently labelled membranes of cells due to cell's irregular shape, variability in size and dynamic movement across Z planes making it difficult to detect and track them. Here we introduce a detailed analysis pipeline to perform segmentation with accurate shape information, combined with BTrackmate, a customized codebase of popular ImageJ/Fiji software Trackmate, to perform cell tracking inside the tissue of interest. We developed VollSeg, a new segmentation method able to detect membrane-labelled cells with low signal-to-noise ratio and dense packing. Finally, we also created an interface in Napari, an Euler angle based viewer, to visualize the tracks along a chosen view making it possible to follow a cell along the plane of motion. Importantly, we provide a detailed protocol to implement this pipeline in a new dataset, together with the required Jupyter notebooks. Our codes are open source available at [Git].