Cells tracking in a live zebrafish embryo.
We designed a set of procedures for achieving the tracking of cell nuclei and the identification of cell divisions in live zebrafish embryos using 3D+time images acquired by confocal laser scanning microscopy (CLSM). Our strategy includes image signal enhancement with feature preserving denoising al...
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2007
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1557170X_v_n_p1631_Melani http://hdl.handle.net/20.500.12110/paper_1557170X_v_n_p1631_Melani |
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paper:paper_1557170X_v_n_p1631_Melani2023-06-08T16:23:16Z Cells tracking in a live zebrafish embryo. algorithm animal animal embryo article artificial intelligence automated pattern recognition computer assisted diagnosis confocal microscopy cytology evaluation study fluorescence microscopy histology image enhancement methodology prenatal development reproducibility sensitivity and specificity three dimensional imaging zebra fish Algorithms Animals Artificial Intelligence Embryo, Nonmammalian Image Enhancement Image Interpretation, Computer-Assisted Imaging, Three-Dimensional Microscopy, Confocal Microscopy, Fluorescence Pattern Recognition, Automated Reproducibility of Results Sensitivity and Specificity Zebrafish We designed a set of procedures for achieving the tracking of cell nuclei and the identification of cell divisions in live zebrafish embryos using 3D+time images acquired by confocal laser scanning microscopy (CLSM). Our strategy includes image signal enhancement with feature preserving denoising algorithm, automated identification of the nuclei position, extraction of the optical flow from 3D images sequences and tracking of nuclei. 2007 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1557170X_v_n_p1631_Melani http://hdl.handle.net/20.500.12110/paper_1557170X_v_n_p1631_Melani |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
algorithm animal animal embryo article artificial intelligence automated pattern recognition computer assisted diagnosis confocal microscopy cytology evaluation study fluorescence microscopy histology image enhancement methodology prenatal development reproducibility sensitivity and specificity three dimensional imaging zebra fish Algorithms Animals Artificial Intelligence Embryo, Nonmammalian Image Enhancement Image Interpretation, Computer-Assisted Imaging, Three-Dimensional Microscopy, Confocal Microscopy, Fluorescence Pattern Recognition, Automated Reproducibility of Results Sensitivity and Specificity Zebrafish |
spellingShingle |
algorithm animal animal embryo article artificial intelligence automated pattern recognition computer assisted diagnosis confocal microscopy cytology evaluation study fluorescence microscopy histology image enhancement methodology prenatal development reproducibility sensitivity and specificity three dimensional imaging zebra fish Algorithms Animals Artificial Intelligence Embryo, Nonmammalian Image Enhancement Image Interpretation, Computer-Assisted Imaging, Three-Dimensional Microscopy, Confocal Microscopy, Fluorescence Pattern Recognition, Automated Reproducibility of Results Sensitivity and Specificity Zebrafish Cells tracking in a live zebrafish embryo. |
topic_facet |
algorithm animal animal embryo article artificial intelligence automated pattern recognition computer assisted diagnosis confocal microscopy cytology evaluation study fluorescence microscopy histology image enhancement methodology prenatal development reproducibility sensitivity and specificity three dimensional imaging zebra fish Algorithms Animals Artificial Intelligence Embryo, Nonmammalian Image Enhancement Image Interpretation, Computer-Assisted Imaging, Three-Dimensional Microscopy, Confocal Microscopy, Fluorescence Pattern Recognition, Automated Reproducibility of Results Sensitivity and Specificity Zebrafish |
description |
We designed a set of procedures for achieving the tracking of cell nuclei and the identification of cell divisions in live zebrafish embryos using 3D+time images acquired by confocal laser scanning microscopy (CLSM). Our strategy includes image signal enhancement with feature preserving denoising algorithm, automated identification of the nuclei position, extraction of the optical flow from 3D images sequences and tracking of nuclei. |
title |
Cells tracking in a live zebrafish embryo. |
title_short |
Cells tracking in a live zebrafish embryo. |
title_full |
Cells tracking in a live zebrafish embryo. |
title_fullStr |
Cells tracking in a live zebrafish embryo. |
title_full_unstemmed |
Cells tracking in a live zebrafish embryo. |
title_sort |
cells tracking in a live zebrafish embryo. |
publishDate |
2007 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_1557170X_v_n_p1631_Melani http://hdl.handle.net/20.500.12110/paper_1557170X_v_n_p1631_Melani |
_version_ |
1768544657340366848 |