Abstract

BackgroundThe motivation behind this paper is to aid the automatic phenotyping of mouse embryos, wherein multiple embryos embedded within a single tube were scanned using Magnetic Resonance Imaging (MRI).ResultsOur algorithm, a modified version of the simplex deformable model of Delingette, addresses various issues with deformable models including initialization and inability to adapt to boundary concavities. In addition, it proposes a novel technique for automatic collision detection of multiple objects which are being segmented simultaneously, hence avoiding major leaks into adjacent neighbouring structures. We address the initialization problem by introducing balloon forces which expand the initial spherical models close to the true boundaries of the embryos. This results in models which are less sensitive to initial minimum of two fold after each stage of deformation. To determine collision during segmentation, our unique collision detection algorithm finds the intersection between binary masks created from the deformed models after every few iterations of the deformation and modifies the segmentation parameters accordingly hence avoiding collision.We have segmented six tubes of three dimensional MR images of multiple mouse embryos using our modified deformable model algorithm. We have then validated the results of the our semi-automatic segmentation versus manual segmentation of the same embryos. Our Validation shows that except paws and tails we have been able to segment the mouse embryos with minor error.ConclusionsThis paper describes our novel multiple object segmentation technique with collision detection using a modified deformable model algorithm. Further, it presents the results of segmenting magnetic resonance images of up to 32 mouse embryos stacked in one gel filled test tube and creating 32 individual masks.

Highlights

  • The motivation behind this paper is to aid the automatic phenotyping of mouse embryos, wherein multiple embryos embedded within a single tube were scanned using Magnetic Resonance Imaging (MRI)

  • * Correspondence: baghdadi@phenogenomics.ca 1Mouse Imaging Centre, The Hospital for Sick Children, Toronto, Canada Full list of author information is available at the end of the article. This encompasses either separate transmit/receive coils for each mouse [2], or packing multiple specimen into the same field of view while using a single coil. The latter strategy was chosen by Schneider et al for phenotyping mouse embryos, placing 32 fixed specimen embedded in gel into a single tube which was imaged using high-resolution MRI at 9.4 Tesla [3]

  • We demonstrate a semi-automatic multiple embryo segmentation technique which allows us to create individual masks for all embryos starting from identical spheres

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Summary

Introduction

The motivation behind this paper is to aid the automatic phenotyping of mouse embryos, wherein multiple embryos embedded within a single tube were scanned using Magnetic Resonance Imaging (MRI). Parallelization of MRI experiments is one technique to compensate for the long imaging time This encompasses either separate transmit/receive coils for each mouse [2], or packing multiple specimen into the same field of view while using a single coil. The latter strategy was chosen by Schneider et al for phenotyping mouse embryos, placing 32 fixed specimen embedded in gel into a single tube which was imaged using high-resolution MRI at 9.4 Tesla [3]

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