1,594 research outputs found
Navigation of brain networks
Understanding the mechanisms of neural communication in large-scale brain
networks remains a major goal in neuroscience. We investigated whether
navigation is a parsimonious routing model for connectomics. Navigating a
network involves progressing to the next node that is closest in distance to a
desired destination. We developed a measure to quantify navigation efficiency
and found that connectomes in a range of mammalian species (human, mouse and
macaque) can be successfully navigated with near-optimal efficiency (>80% of
optimal efficiency for typical connection densities). Rewiring network topology
or repositioning network nodes resulted in 45%-60% reductions in navigation
performance. Specifically, we found that brain networks cannot be progressively
rewired (randomized or clusterized) to result in topologies with significantly
improved navigation performance. Navigation was also found to: i) promote a
resource-efficient distribution of the information traffic load, potentially
relieving communication bottlenecks; and, ii) explain significant variation in
functional connectivity. Unlike prevalently studied communication strategies in
connectomics, navigation does not mandate biologically unrealistic assumptions
about global knowledge of network topology. We conclude that the wiring and
spatial embedding of brain networks is conducive to effective decentralized
communication. Graph-theoretic studies of the connectome should consider
measures of network efficiency and centrality that are consistent with
decentralized models of neural communication
Generative models of the human connectome
The human connectome represents a network map of the brain's wiring diagram
and the pattern into which its connections are organized is thought to play an
important role in cognitive function. The generative rules that shape the
topology of the human connectome remain incompletely understood. Earlier work
in model organisms has suggested that wiring rules based on geometric
relationships (distance) can account for many but likely not all topological
features. Here we systematically explore a family of generative models of the
human connectome that yield synthetic networks designed according to different
wiring rules combining geometric and a broad range of topological factors. We
find that a combination of geometric constraints with a homophilic attachment
mechanism can create synthetic networks that closely match many topological
characteristics of individual human connectomes, including features that were
not included in the optimization of the generative model itself. We use these
models to investigate a lifespan dataset and show that, with age, the model
parameters undergo progressive changes, suggesting a rebalancing of the
generative factors underlying the connectome across the lifespan.Comment: 38 pages, 5 figures + 19 supplemental figures, 1 tabl
Dwelling Quietly in the Rich Club: Brain Network Determinants of Slow Cortical Fluctuations
For more than a century, cerebral cartography has been driven by
investigations of structural and morphological properties of the brain across
spatial scales and the temporal/functional phenomena that emerge from these
underlying features. The next era of brain mapping will be driven by studies
that consider both of these components of brain organization simultaneously --
elucidating their interactions and dependencies. Using this guiding principle,
we explored the origin of slowly fluctuating patterns of synchronization within
the topological core of brain regions known as the rich club, implicated in the
regulation of mood and introspection. We find that a constellation of densely
interconnected regions that constitute the rich club (including the anterior
insula, amygdala, and precuneus) play a central role in promoting a stable,
dynamical core of spontaneous activity in the primate cortex. The slow time
scales are well matched to the regulation of internal visceral states,
corresponding to the somatic correlates of mood and anxiety. In contrast, the
topology of the surrounding "feeder" cortical regions show unstable, rapidly
fluctuating dynamics likely crucial for fast perceptual processes. We discuss
these findings in relation to psychiatric disorders and the future of
connectomics.Comment: 35 pages, 6 figure
A morphospace of functional configuration to assess configural breadth based on brain functional networks
The best approach to quantify human brain functional reconfigurations in
response to varying cognitive demands remains an unresolved topic in network
neuroscience. We propose that such functional reconfigurations may be
categorized into three different types: i) Network Configural Breadth, ii)
Task-to-Task transitional reconfiguration, and iii) Within-Task
reconfiguration. In order to quantify these reconfigurations, we propose a
mesoscopic framework focused on functional networks (FNs) or communities. To do
so, we introduce a 2D network morphospace that relies on two novel mesoscopic
metrics, Trapping Efficiency (TE) and Exit Entropy (EE), which capture topology
and integration of information within and between a reference set of FNs. In
this study, we use this framework to quantify the Network Configural Breadth
across different tasks. We show that the metrics defining this morphospace can
differentiate FNs, cognitive tasks and subjects. We also show that network
configural breadth significantly predicts behavioral measures, such as episodic
memory, verbal episodic memory, fluid intelligence and general intelligence. In
essence, we put forth a framework to explore the cognitive space in a
comprehensive manner, for each individual separately, and at different levels
of granularity. This tool that can also quantify the FN reconfigurations that
result from the brain switching between mental states.Comment: main article: 24 pages, 8 figures, 2 tables. supporting information:
11 pages, 5 figure
Geometry Processing of Conventionally Produced Mouse Brain Slice Images
Brain mapping research in most neuroanatomical laboratories relies on
conventional processing techniques, which often introduce histological
artifacts such as tissue tears and tissue loss. In this paper we present
techniques and algorithms for automatic registration and 3D reconstruction of
conventionally produced mouse brain slices in a standardized atlas space. This
is achieved first by constructing a virtual 3D mouse brain model from annotated
slices of Allen Reference Atlas (ARA). Virtual re-slicing of the reconstructed
model generates ARA-based slice images corresponding to the microscopic images
of histological brain sections. These image pairs are aligned using a geometric
approach through contour images. Histological artifacts in the microscopic
images are detected and removed using Constrained Delaunay Triangulation before
performing global alignment. Finally, non-linear registration is performed by
solving Laplace's equation with Dirichlet boundary conditions. Our methods
provide significant improvements over previously reported registration
techniques for the tested slices in 3D space, especially on slices with
significant histological artifacts. Further, as an application we count the
number of neurons in various anatomical regions using a dataset of 51
microscopic slices from a single mouse brain. This work represents a
significant contribution to this subfield of neuroscience as it provides tools
to neuroanatomist for analyzing and processing histological data.Comment: 14 pages, 11 figure
Resolving Structure in Human Brain Organization: Identifying Mesoscale Organization in Weighted Network Representations
Human brain anatomy and function display a combination of modular and
hierarchical organization, suggesting the importance of both cohesive
structures and variable resolutions in the facilitation of healthy cognitive
processes. However, tools to simultaneously probe these features of brain
architecture require further development. We propose and apply a set of methods
to extract cohesive structures in network representations of brain connectivity
using multi-resolution techniques. We employ a combination of soft
thresholding, windowed thresholding, and resolution in community detection,
that enable us to identify and isolate structures associated with different
weights. One such mesoscale structure is bipartivity, which quantifies the
extent to which the brain is divided into two partitions with high connectivity
between partitions and low connectivity within partitions. A second,
complementary mesoscale structure is modularity, which quantifies the extent to
which the brain is divided into multiple communities with strong connectivity
within each community and weak connectivity between communities. Our methods
lead to multi-resolution curves of these network diagnostics over a range of
spatial, geometric, and structural scales. For statistical comparison, we
contrast our results with those obtained for several benchmark null models. Our
work demonstrates that multi-resolution diagnostic curves capture complex
organizational profiles in weighted graphs. We apply these methods to the
identification of resolution-specific characteristics of healthy weighted graph
architecture and altered connectivity profiles in psychiatric disease.Comment: Comments welcom
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