dc.contributor.author |
Mabaso, M
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dc.contributor.author |
Twala, B
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dc.contributor.author |
Withey, Daniel J
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dc.date.accessioned |
2018-05-18T11:28:43Z |
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dc.date.available |
2018-05-18T11:28:43Z |
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dc.date.issued |
2013-09 |
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dc.identifier.citation |
Mabaso, M., Twala, B. and Withey, D.J. 2013. Quantitative comparison of two particle tracking methods in fluorescence microscopy images. BRICS-CCI & CBIC 2013, Brazil, 8-11 September 2013 |
en_US |
dc.identifier.isbn |
978-1-4799-3194-1 |
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dc.identifier.uri |
https://ieeexplore.ieee.org/document/6855915/
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dc.identifier.uri |
DOI: 10.1109/BRICS-CCI-CBIC.2013.106
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dc.identifier.uri |
http://hdl.handle.net/10204/10220
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dc.description |
Copyright: 2013 IEEE. Due to copyright restrictions, the attached PDF file contains the accepted version of the published item. For access to the published item, please consult the publisher's website. |
en_US |
dc.description.abstract |
Tracking of multiple bright particles (spots) in fluorescence microscopy image sequences is seen as a crucial step in understanding complex information in the cell. However, fluorescence microscopy generates high a volume of noisy image data that cannot be analysed efficiently by means of manual analysis. In this study we compare the performance of two computer-based tracking methods for tracking of bright particles in fluorescence microscopy image sequences. The methods under comparison are, Interacting Multiple Model filter and Feature Point Tracking. The performance of the methods is validated using synthetic but realistic image sequences and real images. The results from experiments show that the Interacting Multiple Model filter performed best, under the test conditions. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
IEEE |
en_US |
dc.relation.ispartofseries |
Worklist;11662 |
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dc.subject |
Fluorescence microscopy images |
en_US |
dc.subject |
Feature Point Tracking |
en_US |
dc.subject |
Interacting Multiple Model filter |
en_US |
dc.subject |
Electrical engineering |
en_US |
dc.title |
Quantitative comparison of two particle tracking methods in fluorescence microscopy images |
en_US |
dc.type |
Conference Presentation |
en_US |
dc.identifier.apacitation |
Mabaso, M., Twala, B., & Withey, D. J. (2013). Quantitative comparison of two particle tracking methods in fluorescence microscopy images. IEEE. http://hdl.handle.net/10204/10220 |
en_ZA |
dc.identifier.chicagocitation |
Mabaso, M, B Twala, and Daniel J Withey. "Quantitative comparison of two particle tracking methods in fluorescence microscopy images." (2013): http://hdl.handle.net/10204/10220 |
en_ZA |
dc.identifier.vancouvercitation |
Mabaso M, Twala B, Withey DJ, Quantitative comparison of two particle tracking methods in fluorescence microscopy images; IEEE; 2013. http://hdl.handle.net/10204/10220 . |
en_ZA |
dc.identifier.ris |
TY - Conference Presentation
AU - Mabaso, M
AU - Twala, B
AU - Withey, Daniel J
AB - Tracking of multiple bright particles (spots) in fluorescence microscopy image sequences is seen as a crucial step in understanding complex information in the cell. However, fluorescence microscopy generates high a volume of noisy image data that cannot be analysed efficiently by means of manual analysis. In this study we compare the performance of two computer-based tracking methods for tracking of bright particles in fluorescence microscopy image sequences. The methods under comparison are, Interacting Multiple Model filter and Feature Point Tracking. The performance of the methods is validated using synthetic but realistic image sequences and real images. The results from experiments show that the Interacting Multiple Model filter performed best, under the test conditions.
DA - 2013-09
DB - ResearchSpace
DP - CSIR
KW - Fluorescence microscopy images
KW - Feature Point Tracking
KW - Interacting Multiple Model filter
KW - Electrical engineering
LK - https://researchspace.csir.co.za
PY - 2013
SM - 978-1-4799-3194-1
T1 - Quantitative comparison of two particle tracking methods in fluorescence microscopy images
TI - Quantitative comparison of two particle tracking methods in fluorescence microscopy images
UR - http://hdl.handle.net/10204/10220
ER -
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en_ZA |