All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

On Proper Simulation of Chromatin Structure in Static Images As Well As in Time-Lapse Sequences in Fluorescence Microscopy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14330%2F15%3A00080650" target="_blank" >RIV/00216224:14330/15:00080650 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1109/ISBI.2015.7163972" target="_blank" >http://dx.doi.org/10.1109/ISBI.2015.7163972</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1109/ISBI.2015.7163972" target="_blank" >10.1109/ISBI.2015.7163972</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    On Proper Simulation of Chromatin Structure in Static Images As Well As in Time-Lapse Sequences in Fluorescence Microscopy

  • Original language description

    In fluorescence microscopy, where the benchmark datasets for validating the various image analysis methods are difficult to obtain, a great demand is either for manually annotated real image data or for computer generated ones. In the last two decades, the latter case has become more and more accessible due to an increasing computer capabilities. However, the development of elaborate models, especially in the field of fluorescence microscopy imaging, is less progressive. In this paper, we propose a novel approach, based on well established concepts, to properly imitate the structure of chromatin inside the cell nucleus as well as its dynamics. The performance of the approach was quantitatively evaluated against the real data. The results show that theproduced images are sufficiently plausible and visually resemble their real counter parts, both for fixed and living cells.

  • Czech name

  • Czech description

Classification

  • Type

    D - Article in proceedings

  • CEP classification

    IN - Informatics

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA14-22461S" target="_blank" >GA14-22461S: Development and Study of Methods for Live Cell Quantification</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Article name in the collection

    Proceedings of 2015 IEEE International Symposium on Biomedical Imaging

  • ISBN

    9781479923748

  • ISSN

    1945-7928

  • e-ISSN

  • Number of pages

    5

  • Pages from-to

    712-716

  • Publisher name

    Engineering in Medicine and Biology Society

  • Place of publication

    Stoughton (WI, USA)

  • Event location

    New York

  • Event date

    Jan 1, 2015

  • Type of event by nationality

    WRD - Celosvětová akce

  • UT code for WoS article