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Model-Based Generation of Synthetic 3D Time-Lapse Sequences of Multiple Mutually Interacting Motile Cells with Filopodia

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14330%2F18%3A00101086" target="_blank" >RIV/00216224:14330/18:00101086 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1007/978-3-030-00536-8_8" target="_blank" >http://dx.doi.org/10.1007/978-3-030-00536-8_8</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/978-3-030-00536-8_8" target="_blank" >10.1007/978-3-030-00536-8_8</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Model-Based Generation of Synthetic 3D Time-Lapse Sequences of Multiple Mutually Interacting Motile Cells with Filopodia

  • Original language description

    Complementing collections of 3D time-lapse image data with comprehensive manual annotations is an extremely laborious and often impracticable task, which hinders objective benchmarking of bioimage analysis workflows as well as training of widespread deep-learning-based approaches. In this paper, we present a novel simulation system capable of generating synthetic 3D time-lapse sequences of multiple mutually interacting cells with filopodial protrusions, accompanied by inherently generated reference annotations, in order to stimulate the development of fully 3D bioimage analysis workflows for filopodium segmentation and tracking in complex scenarios with multiple mutually interacting cells. The system integrates its predecessor, which was designed for single-cell, collision-unaware scenarios only, with proactive, mechanics-based handling of collisions between multiple filopodia, multiple cell bodies, or their combinations. We demonstrate its potential on two generated 3D time-lapse sequences of multiple lung cancer cells with curvilinear filopodia, which visually resemble confocal fluorescence microscopy image data.

  • Czech name

  • Czech description

Classification

  • Type

    D - Article in proceedings

  • CEP classification

  • OECD FORD branch

    10201 - Computer sciences, information science, bioinformathics (hardware development to be 2.2, social aspect to be 5.8)

Result continuities

  • Project

    <a href="/en/project/GJ16-03909Y" target="_blank" >GJ16-03909Y: Development of Reliable Methods for Automated Quantitative Characterization of Cell Motility in Fluorescence Microscopy</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Article name in the collection

    Simulation and Synthesis in Medical Imaging

  • ISBN

    9783030005351

  • ISSN

    0302-9743

  • e-ISSN

  • Number of pages

    9

  • Pages from-to

    71-79

  • Publisher name

    Springer

  • Place of publication

    Cham

  • Event location

    Granada, Spain

  • Event date

    Jan 1, 2018

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article

    000477752900008