Difference between revisions of "Publications/puybareau.17.isbi"
From LRDE
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| booktitle = Proceedings of the IEEE International Symposium on Bio-Medical Imaging (ISBI) |
| booktitle = Proceedings of the IEEE International Symposium on Bio-Medical Imaging (ISBI) |
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| address = Melbourne, Australia |
| address = Melbourne, Australia |
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− | | abstract = Many bio-medical applications involve the analysis of |
+ | | abstract = Many bio-medical applications involve the analysis of sequences for motion characterization. In this article, we consider 2D+t sequences where a particular motion (e.g. a blood flow) is associated with a specific area of the 2D image (e.g. an artery) but multiple motions may exist simultaneously in the same sequences (e.g. there may be several blood vessels present, each with their specific flow). The characterization of this type of motion typically involves first finding the areas where motion is present, followed by an analysis of these motions: speedregularity, frequency, etc. In this article, we propose a methodology called "area-of-motion characterization" suitable for simultaneously detecting and characterizing areas where motion is present in a sequence. We can then classify this motion into consistent areas using unsupervised learning and produce directly usable metrics for various ap- plications. We illustrate this methodology for the analysis of cilia motion on ex-vivo human samplesand we apply and validate the same methodology for blood flow analysis in fish embryo. |
| lrdepaper = http://www.lrde.epita.fr/dload/papers/puybareau.17.isbi.pdf |
| lrdepaper = http://www.lrde.epita.fr/dload/papers/puybareau.17.isbi.pdf |
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| lrdekeywords = Image |
| lrdekeywords = Image |
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| lrdenewsdate = 2017-02-20 |
| lrdenewsdate = 2017-02-20 |
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− | | note = To appear |
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| type = inproceedings |
| type = inproceedings |
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| id = puybareau.17.isbi |
| id = puybareau.17.isbi |
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address = <nowiki>{</nowiki>Melbourne, Australia<nowiki>}</nowiki>, |
address = <nowiki>{</nowiki>Melbourne, Australia<nowiki>}</nowiki>, |
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month = apr, |
month = apr, |
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− | abstract = <nowiki>{</nowiki>Many bio-medical applications involve the analysis of |
+ | abstract = <nowiki>{</nowiki>Many bio-medical applications involve the analysis of |
− | + | sequences for motion characterization. In this article, we |
|
− | + | consider 2D+t sequences where a particular motion (e.g. a |
|
blood flow) is associated with a specific area of the 2D |
blood flow) is associated with a specific area of the 2D |
||
image (e.g. an artery) but multiple motions may exist |
image (e.g. an artery) but multiple motions may exist |
||
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present, followed by an analysis of these motions: speed, |
present, followed by an analysis of these motions: speed, |
||
regularity, frequency, etc. In this article, we propose a |
regularity, frequency, etc. In this article, we propose a |
||
− | methodology called "area-of-motion |
+ | methodology called "area-of-motion characterization" |
suitable for simultaneously detecting and characterizing |
suitable for simultaneously detecting and characterizing |
||
areas where motion is present in a sequence. We can then |
areas where motion is present in a sequence. We can then |
||
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for the analysis of cilia motion on ex-vivo human samples, |
for the analysis of cilia motion on ex-vivo human samples, |
||
and we apply and validate the same methodology for blood |
and we apply and validate the same methodology for blood |
||
− | flow analysis in fish embryo.<nowiki>}</nowiki> |
+ | flow analysis in fish embryo.<nowiki>}</nowiki> |
− | note = <nowiki>{</nowiki>To appear<nowiki>}</nowiki> |
||
<nowiki>}</nowiki> |
<nowiki>}</nowiki> |
||
Revision as of 14:46, 23 August 2017
- Authors
- Elodie Puybareau, Hugues Talbot, Laurent Najman
- Where
- Proceedings of the IEEE International Symposium on Bio-Medical Imaging (ISBI)
- Place
- Melbourne, Australia
- Type
- inproceedings
- Keywords
- Image
- Date
- 2017-02-20
Abstract
Many bio-medical applications involve the analysis of sequences for motion characterization. In this article, we consider 2D+t sequences where a particular motion (e.g. a blood flow) is associated with a specific area of the 2D image (e.g. an artery) but multiple motions may exist simultaneously in the same sequences (e.g. there may be several blood vessels present, each with their specific flow). The characterization of this type of motion typically involves first finding the areas where motion is present, followed by an analysis of these motions: speedregularity, frequency, etc. In this article, we propose a methodology called "area-of-motion characterization" suitable for simultaneously detecting and characterizing areas where motion is present in a sequence. We can then classify this motion into consistent areas using unsupervised learning and produce directly usable metrics for various ap- plications. We illustrate this methodology for the analysis of cilia motion on ex-vivo human samplesand we apply and validate the same methodology for blood flow analysis in fish embryo.
Documents
Bibtex (lrde.bib)
@InProceedings{ puybareau.17.isbi, author = {Elodie Puybareau and Hugues Talbot and Laurent Najman}, title = {Periodic Area-of-Motion characterization for Bio-Medical applications}, booktitle = {Proceedings of the IEEE International Symposium on Bio-Medical Imaging (ISBI)}, year = 2017, address = {Melbourne, Australia}, month = apr, abstract = {Many bio-medical applications involve the analysis of sequences for motion characterization. In this article, we consider 2D+t sequences where a particular motion (e.g. a blood flow) is associated with a specific area of the 2D image (e.g. an artery) but multiple motions may exist simultaneously in the same sequences (e.g. there may be several blood vessels present, each with their specific flow). The characterization of this type of motion typically involves first finding the areas where motion is present, followed by an analysis of these motions: speed, regularity, frequency, etc. In this article, we propose a methodology called "area-of-motion characterization" suitable for simultaneously detecting and characterizing areas where motion is present in a sequence. We can then classify this motion into consistent areas using unsupervised learning and produce directly usable metrics for various ap- plications. We illustrate this methodology for the analysis of cilia motion on ex-vivo human samples, and we apply and validate the same methodology for blood flow analysis in fish embryo.} }