Multi-object segmentation algorithms are of great interest in a very large range of fields. Deep learning brought major improvements in terms of processing speed or prediction accuracy. Nevertheless, some traditional methods such as active surfaces have features that conventional deep learning methods cannot provide, especially representing the object in a continuous geometrical way and encoding prior information on the shapes to segment. Those features are of particular interest in biology to efficiently segment noisy and poorly resolved data, and then understand the interactions between segmented cells. We introduce NAGINI-3D (N-Active shapes for seGmentINg 3D biological Images), a new hybrid segmentation method dedicated to multi-object segmentation of 3D images that combines the efficiency of deep learning and the powerful representation of active surfaces. We evaluate our method on real and synthetic 3D datasets of fluorescence microscopy.

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Prediction of Parametric Surfaces for Multi-object Segmentation in 3D Biological Imaging

  • Quentin Rapilly,
  • Anaïs Badoual,
  • Pierre Maindron,
  • Guenaelle Bouet,
  • Charles Kervrann

摘要

Multi-object segmentation algorithms are of great interest in a very large range of fields. Deep learning brought major improvements in terms of processing speed or prediction accuracy. Nevertheless, some traditional methods such as active surfaces have features that conventional deep learning methods cannot provide, especially representing the object in a continuous geometrical way and encoding prior information on the shapes to segment. Those features are of particular interest in biology to efficiently segment noisy and poorly resolved data, and then understand the interactions between segmented cells. We introduce NAGINI-3D (N-Active shapes for seGmentINg 3D biological Images), a new hybrid segmentation method dedicated to multi-object segmentation of 3D images that combines the efficiency of deep learning and the powerful representation of active surfaces. We evaluate our method on real and synthetic 3D datasets of fluorescence microscopy.