Detailed Information on Publication Record
2017
Model-Based Generation of Synthetic 3D Time-Lapse Sequences of Motile Cells with Growing Filopodia
SOROKIN, Dmitry, Igor PETERLÍK, Vladimír ULMAN, David SVOBODA, Martin MAŠKA et. al.Basic information
Original name
Model-Based Generation of Synthetic 3D Time-Lapse Sequences of Motile Cells with Growing Filopodia
Authors
SOROKIN, Dmitry (643 Russian Federation, guarantor, belonging to the institution), Igor PETERLÍK (703 Slovakia, belonging to the institution), Vladimír ULMAN (203 Czech Republic, belonging to the institution), David SVOBODA (203 Czech Republic, belonging to the institution) and Martin MAŠKA (203 Czech Republic, belonging to the institution)
Edition
Melbourne, 14th IEEE International Symposium on Biomedical Imaging, p. 822-826, 5 pp. 2017
Publisher
IEEE
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10201 Computer sciences, information science, bioinformatics
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
electronic version available online
References:
RIV identification code
RIV/00216224:14330/17:00094698
Organization unit
Faculty of Informatics
ISBN
978-1-5090-1172-8
ISSN
UT WoS
000414283200191
Keywords in English
Simulation; 3D time-lapse sequence; synthetic cell; cell deformation; filopodium evolution
Tags
International impact, Reviewed
Změněno: 27/4/2018 11:10, RNDr. Pavel Šmerk, Ph.D.
Abstract
V originále
The existence of benchmark datasets is essential to objectively evaluate various image analysis methods. Nevertheless, manual annotations of fluorescence microscopy image data are very laborious and not often practicable, especially in the case of 3D+t experiments. In this work, we propose a simulation system capable of generating 3D time-lapse sequences of single motile cells with filopodial protrusions, accompanied by inherently generated ground truth. The system consists of three globally synchronized modules, each responsible for a separate task: the evolution of filopodia on a molecular level, linear elastic deformation of the entire cell with filopodia, and generation of realistic, time-coherent cell texture. The capability of our system is demonstrated by generating a synthetic 3D time-lapse sequence of a single lung cancer cell with two growing filopodia, visually resembling its real counterpart acquired using a confocal fluorescence microscope.
Links
GJ16-03909Y, research and development project |
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