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Visualizing Stable Features in Live Cell Nucleus for Evaluation of the Cell Global Motion Compensation

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    SYSNO ASEP0435958
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleVisualizing Stable Features in Live Cell Nucleus for Evaluation of the Cell Global Motion Compensation
    Author(s) Sorokin, D.V. (CZ)
    Suchánková, Jana (BFU-R)
    Bártová, Eva (BFU-R) ORCID
    Matula, P. (CZ)
    Number of authors4
    Source TitleFolia Biologica. - : Univerzita Karlova v Praze - ISSN 0015-5500
    Roč. 60, č. 1 (2014), s. 45-49
    Number of pages5 s.
    Publication formPrint - P
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordscell global motion compensation ; UV laser bleaching ; image registration
    Subject RIVBO - Biophysics
    R&D ProjectsGBP302/12/G157 GA ČR - Czech Science Foundation (CSF)
    EE2.3.30.0030 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportBFU-R - RVO:68081707
    UT WOS000343275800007
    AnnotationThe compensation of cell motion is an important step in single-particle tracking analysis of live cells. This step is required in most of the cases, since the movement of subcellular foci is superimposed by the movement and deformation of the cell, while only the local motion of the foci is important to be analysed. The cell motion and deformation compensation is usually performed by means of image registration. There are a number of approaches with different models and properties presented in the literature that perform cell image registration. However, the evaluation of the registration approach quality on real data is a tricky problem due to the fact that some stable features in the images with a priori no local motion are needed. In this paper we propose a methodology for creating live cell nuclei image sequences with stable features imposed. The features are defined using the regions of fluorescence bleaching invoked by the UV laser. Data with different deformations are acquired and can be used for evaluation of the cell image registration methods. Along with that, we describe an image analysis technique and a metric that can characterize the quality of the method quantitatively.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2015
Number of the records: 1  

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