18,707 research outputs found
Resolving structural variability in network models and the brain
Large-scale white matter pathways crisscrossing the cortex create a complex
pattern of connectivity that underlies human cognitive function. Generative
mechanisms for this architecture have been difficult to identify in part
because little is known about mechanistic drivers of structured networks. Here
we contrast network properties derived from diffusion spectrum imaging data of
the human brain with 13 synthetic network models chosen to probe the roles of
physical network embedding and temporal network growth. We characterize both
the empirical and synthetic networks using familiar diagnostics presented in
statistical form, as scatter plots and distributions, to reveal the full range
of variability of each measure across scales in the network. We focus on the
degree distribution, degree assortativity, hierarchy, topological Rentian
scaling, and topological fractal scaling---in addition to several summary
statistics, including the mean clustering coefficient, shortest path length,
and network diameter. The models are investigated in a progressive, branching
sequence, aimed at capturing different elements thought to be important in the
brain, and range from simple random and regular networks, to models that
incorporate specific growth rules and constraints. We find that synthetic
models that constrain the network nodes to be embedded in anatomical brain
regions tend to produce distributions that are similar to those extracted from
the brain. We also find that network models hardcoded to display one network
property do not in general also display a second, suggesting that multiple
neurobiological mechanisms might be at play in the development of human brain
network architecture. Together, the network models that we develop and employ
provide a potentially useful starting point for the statistical inference of
brain network structure from neuroimaging data.Comment: 24 pages, 11 figures, 1 table, supplementary material
The Small World of Osteocytes: Connectomics of the Lacuno-Canalicular Network in Bone
Osteocytes and their cell processes reside in a large, interconnected network
of voids pervading the mineralized bone matrix of most vertebrates. This
osteocyte lacuno-canalicular network (OLCN) is believed to play important roles
in mechanosensing, mineral homeostasis, and for the mechanical properties of
bone. While the extracellular matrix structure of bone is extensively studied
on ultrastructural and macroscopic scales, there is a lack of quantitative
knowledge on how the cellular network is organized. Using a recently introduced
imaging and quantification approach, we analyze the OLCN in different bone
types from mouse and sheep that exhibit different degrees of structural
organization not only of the cell network but also of the fibrous matrix
deposited by the cells. We define a number of robust, quantitative measures
that are derived from the theory of complex networks. These measures enable us
to gain insights into how efficient the network is organized with regard to
intercellular transport and communication. Our analysis shows that the cell
network in regularly organized, slow-growing bone tissue from sheep is less
connected, but more efficiently organized compared to irregular and
fast-growing bone tissue from mice. On the level of statistical topological
properties (edges per node, edge length and degree distribution), both network
types are indistinguishable, highlighting that despite pronounced differences
at the tissue level, the topological architecture of the osteocyte canalicular
network at the subcellular level may be independent of species and bone type.
Our results suggest a universal mechanism underlying the self-organization of
individual cells into a large, interconnected network during bone formation and
mineralization
Persistent Homology in Sparse Regression and its Application to Brain Morphometry
Sparse systems are usually parameterized by a tuning parameter that
determines the sparsity of the system. How to choose the right tuning parameter
is a fundamental and difficult problem in learning the sparse system. In this
paper, by treating the the tuning parameter as an additional dimension,
persistent homological structures over the parameter space is introduced and
explored. The structures are then further exploited in speeding up the
computation using the proposed soft-thresholding technique. The topological
structures are further used as multivariate features in the tensor-based
morphometry (TBM) in characterizing white matter alterations in children who
have experienced severe early life stress and maltreatment. These analyses
reveal that stress-exposed children exhibit more diffuse anatomical
organization across the whole white matter region.Comment: submitted to IEEE Transactions on Medical Imagin
Graph analysis of functional brain networks: practical issues in translational neuroscience
The brain can be regarded as a network: a connected system where nodes, or
units, represent different specialized regions and links, or connections,
represent communication pathways. From a functional perspective communication
is coded by temporal dependence between the activities of different brain
areas. In the last decade, the abstract representation of the brain as a graph
has allowed to visualize functional brain networks and describe their
non-trivial topological properties in a compact and objective way. Nowadays,
the use of graph analysis in translational neuroscience has become essential to
quantify brain dysfunctions in terms of aberrant reconfiguration of functional
brain networks. Despite its evident impact, graph analysis of functional brain
networks is not a simple toolbox that can be blindly applied to brain signals.
On the one hand, it requires a know-how of all the methodological steps of the
processing pipeline that manipulates the input brain signals and extract the
functional network properties. On the other hand, a knowledge of the neural
phenomenon under study is required to perform physiological-relevant analysis.
The aim of this review is to provide practical indications to make sense of
brain network analysis and contrast counterproductive attitudes
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
- …