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 / C.Melani; M.Campana; B.Lombardot; B.Rizzi; F.Veronesi; C.Zanella; P.Bourgine; K.Mikula; N.Peyrieras; A.Sarti;. - STAMPA. - 1:(2007), pp. 1631-1634. (Intervento presentato al convegno 29th IEEE EMBS Annual International Conference in 2007 in Lyon tenutosi a Lyon nel August 23-26, 2007).
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 nucleiI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
