Detailed Information on Publication Record
2015
On Proper Simulation of Chromatin Structure in Static Images As Well As in Time-Lapse Sequences in Fluorescence Microscopy
SVOBODA, David, Vladimír ULMAN and Igor PETERLÍKBasic information
Original name
On Proper Simulation of Chromatin Structure in Static Images As Well As in Time-Lapse Sequences in Fluorescence Microscopy
Authors
SVOBODA, David (203 Czech Republic, guarantor, belonging to the institution), Vladimír ULMAN (203 Czech Republic, belonging to the institution) and Igor PETERLÍK (703 Slovakia, belonging to the institution)
Edition
Stoughton (WI, USA), Proceedings of 2015 IEEE International Symposium on Biomedical Imaging, p. 712-716, 5 pp. 2015
Publisher
Engineering in Medicine and Biology Society
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
storage medium (CD, DVD, flash disk)
RIV identification code
RIV/00216224:14330/15:00080650
Organization unit
Faculty of Informatics
ISBN
978-1-4799-2374-8
ISSN
UT WoS
000380546000171
Keywords in English
Simulation; Synthetic cell; Chromatin structure; Nucleus deformation; Linear elasticity; FEM
Tags
International impact, Reviewed
Změněno: 16/7/2019 11:11, doc. RNDr. David Svoboda, Ph.D.
Abstract
V originále
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 the produced images are sufficiently plausible and visually resemble their real counter parts, both for fixed and living cells.
Links
GA14-22461S, research and development project |
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