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

Cells tracking in a live zebrafish embryo

SARTI, ALESSANDRO
2007

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
Conference Proceedings IEEE Engineering in Medicine and Biology Society
1631
1634
C.Melani; M.Campana; B.Lombardot; B.Rizzi; F.Veronesi; C.Zanella; P.Bourgine; K.Mikula; N.Peyrieras; A.Sarti;
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/59963
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