Abstract

BackgroundSerial block face scanning electron microscopy (SBFEM) is becoming a popular technology in neuroscience. We have seen in the last years an increasing number of works addressing the problem of segmenting cellular structures in SBFEM images of brain tissue. The vast majority of them is designed to segment one specific structure, typically membranes, synapses and mitochondria. Our hypothesis is that the performance of these algorithms can be improved by concurrently segmenting more than one structure using image descriptions obtained at different scales.ResultsWe consider the simultaneous segmentation of two structures, namely, synapses with mitochondria, and mitochondra with membranes. To this end we select three image stacks encompassing different SBFEM acquisition technologies and image resolutions. We introduce both a new Boosting algorithm to perform feature scale selection and the Jaccard Curve as a tool compare several segmentation results. We then experimentally study the gains in performance obtained when simultaneously segmenting two structures with properly selected image descriptor scales. The results show that by doing so we achieve significant gains in segmentation accuracy when compared to the best results in the literature.ConclusionsSimultaneously segmenting several neuronal structures described at different scales provides voxel classification algorithms with highly discriminating features that significantly improve segmentation accuracy.

Highlights

  • Serial block face scanning electron microscopy (SBFEM) is becoming a popular technology in neuroscience

  • Here we describe the experiments performed to evaluate the image segmentation method described in the previous section

  • In this paper we have presented an algorithm for segmenting mitochondria, synapses and membranes in Serial Block Face Electron Microscopy (SBFEM) images of brain tissue

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Summary

Introduction

Serial block face scanning electron microscopy (SBFEM) is becoming a popular technology in neuroscience. Understanding the structure, connectivity and functionality of the brain is one of the challenges faced by science in the 21st century. This grand challenge is supported by the development of multiple and complementary brain imaging modalities such as structural and functional imaging [1] and light microscopy [2, 3]. Recent advances in SFBEM support this long term goal [4,5,6] They have made it possible to automatically acquire long sequences of high resolution images of the brain at the nanometer scale. In this paper we consider the problem of segmenting mitochondria and synapses that along with membranes are some of the most prominent neuronal structures

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