2,633 research outputs found
Guided Proofreading of Automatic Segmentations for Connectomics
Automatic cell image segmentation methods in connectomics produce merge and
split errors, which require correction through proofreading. Previous research
has identified the visual search for these errors as the bottleneck in
interactive proofreading. To aid error correction, we develop two classifiers
that automatically recommend candidate merges and splits to the user. These
classifiers use a convolutional neural network (CNN) that has been trained with
errors in automatic segmentations against expert-labeled ground truth. Our
classifiers detect potentially-erroneous regions by considering a large context
region around a segmentation boundary. Corrections can then be performed by a
user with yes/no decisions, which reduces variation of information 7.5x faster
than previous proofreading methods. We also present a fully-automatic mode that
uses a probability threshold to make merge/split decisions. Extensive
experiments using the automatic approach and comparing performance of novice
and expert users demonstrate that our method performs favorably against
state-of-the-art proofreading methods on different connectomics datasets.Comment: Supplemental material available at
http://rhoana.org/guidedproofreading/supplemental.pd
Multiscale Exploration of Mouse Brain Microstructures Using the Knife-Edge Scanning Microscope Brain Atlas
Connectomics is the study of the full connection matrix of the brain. Recent advances in high-throughput, high-resolution 3D microscopy methods have enabled the imaging of whole small animal brains at a sub-micrometer resolution, potentially opening the road to full-blown connectomics research. One of the first such instruments to achieve whole-brain-scale imaging at sub-micrometer resolution is the Knife-Edge Scanning Microscope (KESM). KESM whole-brain data sets now include Golgi (neuronal circuits), Nissl (soma distribution), and India ink (vascular networks). KESM data can contribute greatly to connectomics research, since they fill the gap between lower resolution, large volume imaging methods (such as diffusion MRI) and higher resolution, small volume methods (e.g., serial sectioning electron microscopy). Furthermore, KESM data are by their nature multiscale, ranging from the subcellular to the whole organ scale. Due to this, visualization alone is a huge challenge, before we even start worrying about quantitative connectivity analysis. To solve this issue, we developed a web-based neuroinformatics framework for efficient visualization and analysis of the multiscale KESM data sets. In this paper, we will first provide an overview of KESM, then discuss in detail the KESM data sets and the web-based neuroinformatics framework, which is called the KESM brain atlas (KESMBA). Finally, we will discuss the relevance of the KESMBA to connectomics research, and identify challenges and future directions
Mapping hybrid functional-structural connectivity traits in the human connectome
One of the crucial questions in neuroscience is how a rich functional
repertoire of brain states relates to its underlying structural organization.
How to study the associations between these structural and functional layers is
an open problem that involves novel conceptual ways of tackling this question.
We here propose an extension of the Connectivity Independent Component Analysis
(connICA) framework, to identify joint structural-functional connectivity
traits. Here, we extend connICA to integrate structural and functional
connectomes by merging them into common hybrid connectivity patterns that
represent the connectivity fingerprint of a subject. We test this extended
approach on the 100 unrelated subjects from the Human Connectome Project. The
method is able to extract main independent structural-functional connectivity
patterns from the entire cohort that are sensitive to the realization of
different tasks. The hybrid connICA extracted two main task-sensitive hybrid
traits. The first, encompassing the within and between connections of dorsal
attentional and visual areas, as well as fronto-parietal circuits. The second,
mainly encompassing the connectivity between visual, attentional, DMN and
subcortical networks. Overall, these findings confirms the potential ofthe
hybrid connICA for the compression of structural/functional connectomes into
integrated patterns from a set of individual brain networks.Comment: article: 34 pages, 4 figures; supplementary material: 5 pages, 5
figure
Recursive Training of 2D-3D Convolutional Networks for Neuronal Boundary Detection
Efforts to automate the reconstruction of neural circuits from 3D electron
microscopic (EM) brain images are critical for the field of connectomics. An
important computation for reconstruction is the detection of neuronal
boundaries. Images acquired by serial section EM, a leading 3D EM technique,
are highly anisotropic, with inferior quality along the third dimension. For
such images, the 2D max-pooling convolutional network has set the standard for
performance at boundary detection. Here we achieve a substantial gain in
accuracy through three innovations. Following the trend towards deeper networks
for object recognition, we use a much deeper network than previously employed
for boundary detection. Second, we incorporate 3D as well as 2D filters, to
enable computations that use 3D context. Finally, we adopt a recursively
trained architecture in which a first network generates a preliminary boundary
map that is provided as input along with the original image to a second network
that generates a final boundary map. Backpropagation training is accelerated by
ZNN, a new implementation of 3D convolutional networks that uses multicore CPU
parallelism for speed. Our hybrid 2D-3D architecture could be more generally
applicable to other types of anisotropic 3D images, including video, and our
recursive framework for any image labeling problem
Annotating Synapses in Large EM Datasets
Reconstructing neuronal circuits at the level of synapses is a central
problem in neuroscience and becoming a focus of the emerging field of
connectomics. To date, electron microscopy (EM) is the most proven technique
for identifying and quantifying synaptic connections. As advances in EM make
acquiring larger datasets possible, subsequent manual synapse identification
({\em i.e.}, proofreading) for deciphering a connectome becomes a major time
bottleneck. Here we introduce a large-scale, high-throughput, and
semi-automated methodology to efficiently identify synapses. We successfully
applied our methodology to the Drosophila medulla optic lobe, annotating many
more synapses than previous connectome efforts. Our approaches are extensible
and will make the often complicated process of synapse identification
accessible to a wider-community of potential proofreaders
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