613 research outputs found
Synaptic partner prediction from point annotations in insect brains
High-throughput electron microscopy allows recording of lar- ge stacks of
neural tissue with sufficient resolution to extract the wiring diagram of the
underlying neural network. Current efforts to automate this process focus
mainly on the segmentation of neurons. However, in order to recover a wiring
diagram, synaptic partners need to be identi- fied as well. This is especially
challenging in insect brains like Drosophila melanogaster, where one
presynaptic site is associated with multiple post- synaptic elements. Here we
propose a 3D U-Net architecture to directly identify pairs of voxels that are
pre- and postsynaptic to each other. To that end, we formulate the problem of
synaptic partner identification as a classification problem on long-range edges
between voxels to encode both the presence of a synaptic pair and its
direction. This formulation allows us to directly learn from synaptic point
annotations instead of more ex- pensive voxel-based synaptic cleft or vesicle
annotations. We evaluate our method on the MICCAI 2016 CREMI challenge and
improve over the current state of the art, producing 3% fewer errors than the
next best method
Synaptic Cleft Segmentation in Non-Isotropic Volume Electron Microscopy of the Complete Drosophila Brain
Neural circuit reconstruction at single synapse resolution is increasingly
recognized as crucially important to decipher the function of biological
nervous systems. Volume electron microscopy in serial transmission or scanning
mode has been demonstrated to provide the necessary resolution to segment or
trace all neurites and to annotate all synaptic connections.
Automatic annotation of synaptic connections has been done successfully in
near isotropic electron microscopy of vertebrate model organisms. Results on
non-isotropic data in insect models, however, are not yet on par with human
annotation.
We designed a new 3D-U-Net architecture to optimally represent isotropic
fields of view in non-isotropic data. We used regression on a signed distance
transform of manually annotated synaptic clefts of the CREMI challenge dataset
to train this model and observed significant improvement over the state of the
art.
We developed open source software for optimized parallel prediction on very
large volumetric datasets and applied our model to predict synaptic clefts in a
50 tera-voxels dataset of the complete Drosophila brain. Our model generalizes
well to areas far away from where training data was available
Modeling Brain Circuitry over a Wide Range of Scales
If we are ever to unravel the mysteries of brain function at its most
fundamental level, we will need a precise understanding of how its component
neurons connect to each other. Electron Microscopes (EM) can now provide the
nanometer resolution that is needed to image synapses, and therefore
connections, while Light Microscopes (LM) see at the micrometer resolution
required to model the 3D structure of the dendritic network. Since both the
topology and the connection strength are integral parts of the brain's wiring
diagram, being able to combine these two modalities is critically important.
In fact, these microscopes now routinely produce high-resolution imagery in
such large quantities that the bottleneck becomes automated processing and
interpretation, which is needed for such data to be exploited to its full
potential. In this paper, we briefly review the Computer Vision techniques we
have developed at EPFL to address this need. They include delineating dendritic
arbors from LM imagery, segmenting organelles from EM, and combining the two
into a consistent representation
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