| Literature DB >> 27037463 |
Simon Eck1, Stefan Wörz2, Katharina Müller-Ott3, Matthias Hahn4, Andreas Biesdorf5, Gunnar Schotta4, Karsten Rippe3, Karl Rohr6.
Abstract
The genome is partitioned into regions of euchromatin and heterochromatin. The organization of heterochromatin is important for the regulation of cellular processes such as chromosome segregation and gene silencing, and their misregulation is linked to cancer and other diseases. We present a model-based approach for automatic 3D segmentation and 3D shape analysis of heterochromatin foci from 3D confocal light microscopy images. Our approach employs a novel 3D intensity model based on spherical harmonics, which analytically describes the shape and intensities of the foci. The model parameters are determined by fitting the model to the image intensities using least-squares minimization. To characterize the 3D shape of the foci, we exploit the computed spherical harmonics coefficients and determine a shape descriptor. We applied our approach to 3D synthetic image data as well as real 3D static and real 3D time-lapse microscopy images, and compared the performance with that of previous approaches. It turned out that our approach yields accurate 3D segmentation results and performs better than previous approaches. We also show that our approach can be used for quantifying 3D shape differences of heterochromatin foci.Entities:
Keywords: 3D parametric intensity model; Confocal light microscopy; Pericentric heterochromatin; Spherical harmonics
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Year: 2016 PMID: 27037463 DOI: 10.1016/j.media.2016.03.001
Source DB: PubMed Journal: Med Image Anal ISSN: 1361-8415 Impact factor: 8.545