Multimodal Simulations in Live Cell Imaging

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14330%2F17%3A00095035" target="_blank" >RIV/00216224:14330/17:00095035 - isvavai.cz</a>

Výsledek na webu

<a href="http://dx.doi.org/10.1007/978-3-319-68127-6_10" target="_blank" >http://dx.doi.org/10.1007/978-3-319-68127-6_10</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1007/978-3-319-68127-6_10" target="_blank" >10.1007/978-3-319-68127-6_10</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Multimodal Simulations in Live Cell Imaging

Popis výsledku v původním jazyce

During the last two decades a large amount of new simulation frameworks in the field of cell imaging has emerged. They were expected to serve as performance assessment tools for newly developed as well as for already existing cell segmentation or tracking algorithms. These simulators have typically been designed as single purpose tools. They generate the synthetic image data for one particular modality and one particular cell type. In this study, we introduce a novel multipurpose simulation framework, which produces the synthetic time-lapse image sequences of living endothelial cells for two different modalities: fluorescence and phase contrast microscopy, both in widefield or confocal mode. This may help in evaluating a wider range of desired image processing algorithms across multiple modalities.

Název v anglickém jazyce

Multimodal Simulations in Live Cell Imaging

Popis výsledku anglicky

During the last two decades a large amount of new simulation frameworks in the field of cell imaging has emerged. They were expected to serve as performance assessment tools for newly developed as well as for already existing cell segmentation or tracking algorithms. These simulators have typically been designed as single purpose tools. They generate the synthetic image data for one particular modality and one particular cell type. In this study, we introduce a novel multipurpose simulation framework, which produces the synthetic time-lapse image sequences of living endothelial cells for two different modalities: fluorescence and phase contrast microscopy, both in widefield or confocal mode. This may help in evaluating a wider range of desired image processing algorithms across multiple modalities.

Druh

D - Stať ve sborníku

CEP obor

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OECD FORD obor

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

Projekt

<a href="/cs/project/GA17-05048S" target="_blank" >GA17-05048S: Segmentace a trekování živých buněk v multimodálních obrazech</a><br>

Návaznosti

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

Rok uplatnění

2017

Kód důvěrnosti údajů

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

Název statě ve sborníku

Simulation and Synthesis in Medical Imaging

ISBN

9783319681269

ISSN

0302-9743

e-ISSN

—

Počet stran výsledku

10

Strana od-do

89-98

Název nakladatele

Springer

Místo vydání

Neuveden

Místo konání akce

Québec City, QC, Canada

Datum konání akce

10. 9. 2017

Typ akce podle státní příslušnosti

WRD - Celosvětová akce

Kód UT WoS článku

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