Detailed Information on Publication Record
2015
TRAgen: A Tool for Generation of Synthetic Time-Lapse Image Sequences of Living Cells
ULMAN, Vladimír, Zoltán ORÉMUŠ and David SVOBODABasic information
Original name
TRAgen: A Tool for Generation of Synthetic Time-Lapse Image Sequences of Living Cells
Name in Czech
TRAgen: nástroj pro generování syntetických časosběrných obrazových sekvencí živých buněk
Authors
ULMAN, Vladimír (203 Czech Republic, guarantor, belonging to the institution), Zoltán ORÉMUŠ (703 Slovakia, belonging to the institution) and David SVOBODA (203 Czech Republic, belonging to the institution)
Edition
Heidelberg, Německo, Proceedings of 18th International Conference on Image Analysis and Processing, p. 623-634, 12 pp. 2015
Publisher
Springer International Publishing
Other information
Language
English
Type of outcome
Stať ve sborníku
Field of Study
10201 Computer sciences, information science, bioinformatics
Country of publisher
Germany
Confidentiality degree
není předmětem státního či obchodního tajemství
Publication form
storage medium (CD, DVD, flash disk)
Impact factor
Impact factor: 0.402 in 2005
RIV identification code
RIV/00216224:14330/15:00080843
Organization unit
Faculty of Informatics
ISBN
978-3-319-23230-0
ISSN
UT WoS
000364991200056
Keywords (in Czech)
Biomedical Imaging; Simulation; Evaluation; Cell Tracking
Keywords in English
Biomedical images; Simulations; Evaluation; Cell Tracking
Tags
International impact, Reviewed
Změněno: 7/4/2017 16:56, RNDr. Vladimír Ulman, Ph.D.
Abstract
V originále
In biomedical image processing, correct tracking of individual cells is important task for the study of dynamic cellular processes. It is, however, often difficult to decide whether obtained tracking results are correct or not. This is mainly due to complexity of the data that can show hundreds of cells, due to improper data sampling either in time or in space, or when the time-lapse sequence consists of blurred noisy images. This prohibits manual extraction of reliable ground truth (GT) data as well. Nonetheless, if reliable testing data with GT were available, one could compare the results of the examined tracking algorithm with the GT and assess its performance quantitatively. In this paper, we introduce a novel versatile tool capable of generating 2D image sequences showing simulated living cell populations with GT for evaluation of biomedical tracking. The simulated events include namely cell motion, cell division, and cell clustering up to tissue-level density. The method is primarily designed to operate at inter-cellular scope.
Links
GA14-22461S, research and development project |
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