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.

Recognition and tracking of cells in a live zebrafish embryo

MELANI, CAMILO;CAMPANA, MATTEO;RIZZI, BARBARA;ZANELLA, CECILIA;SARTI, ALESSANDRO
2008

Abstract

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.
Atti del 1° Congresso Nazionale di Bioingegneria
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C. Melani; M. Campana; B. Rizzi; C. Zanella; P. Bourgine; K. Mikula; N. Peyriéras; A. Sarti
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/79798
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