11,035 research outputs found
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
Ensemble tractography
Fiber tractography uses diffusion MRI to estimate the trajectory and cortical projection zones of white matter fascicles in the living human brain. There are many different tractography algorithms and each requires the user to set several parameters, such as curvature threshold. Choosing a single algorithm with a specific parameters sets poses two challenges. First, different algorithms and parameter values produce different results. Second, the optimal choice of algorithm and parameter value may differ between different white matter regions or different fascicles, subjects, and acquisition parameters. We propose using ensemble methods to reduce algorithm and parameter dependencies. To do so we separate the processes of fascicle generation and evaluation. Specifically, we analyze the value of creating optimized connectomes by systematically combining candidate fascicles from an ensemble of algorithms (deterministic and probabilistic) and sweeping through key parameters (curvature and stopping criterion). The ensemble approach leads to optimized connectomes that provide better cross-validatedprediction error of the diffusion MRI data than optimized connectomes generated using the singlealgorithms or parameter set. Furthermore, the ensemble approach produces connectomes that contain both short- and long-range fascicles, whereas single-parameter connectomes are biased towards one or the other. In summary, a systematic ensemble tractography approach can produce connectomes that are superior to standard single parameter estimates both for predicting the diffusion measurements and estimating white matter fascicles.Fil: Takemura, Hiromasa. University of Stanford; Estados Unidos. Osaka University; JapónFil: Caiafa, César Federico. Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Instituto Argentino de Radioastronomía. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto Argentino de Radioastronomía; ArgentinaFil: Wandell, Brian A.. University of Stanford; Estados UnidosFil: Pestilli, Franco. Indiana University; Estados Unido
Simultaneous Matrix Diagonalization for Structural Brain Networks Classification
This paper considers the problem of brain disease classification based on
connectome data. A connectome is a network representation of a human brain. The
typical connectome classification problem is very challenging because of the
small sample size and high dimensionality of the data. We propose to use
simultaneous approximate diagonalization of adjacency matrices in order to
compute their eigenstructures in more stable way. The obtained approximate
eigenvalues are further used as features for classification. The proposed
approach is demonstrated to be efficient for detection of Alzheimer's disease,
outperforming simple baselines and competing with state-of-the-art approaches
to brain disease classification
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
Structural subnetwork evolution across the life-span: rich-club, feeder, seeder
The impact of developmental and aging processes on brain connectivity and the
connectome has been widely studied. Network theoretical measures and certain
topological principles are computed from the entire brain, however there is a
need to separate and understand the underlying subnetworks which contribute
towards these observed holistic connectomic alterations. One organizational
principle is the rich-club - a core subnetwork of brain regions that are
strongly connected, forming a high-cost, high-capacity backbone that is
critical for effective communication in the network. Investigations primarily
focus on its alterations with disease and age. Here, we present a systematic
analysis of not only the rich-club, but also other subnetworks derived from
this backbone - namely feeder and seeder subnetworks. Our analysis is applied
to structural connectomes in a normal cohort from a large, publicly available
lifespan study. We demonstrate changes in rich-club membership with age
alongside a shift in importance from 'peripheral' seeder to feeder subnetworks.
Our results show a refinement within the rich-club structure (increase in
transitivity and betweenness centrality), as well as increased efficiency in
the feeder subnetwork and decreased measures of network integration and
segregation in the seeder subnetwork. These results demonstrate the different
developmental patterns when analyzing the connectome stratified according to
its rich-club and the potential of utilizing this subnetwork analysis to reveal
the evolution of brain architectural alterations across the life-span
Focused Proofreading: Efficiently Extracting Connectomes from Segmented EM Images
Identifying complex neural circuitry from electron microscopic (EM) images
may help unlock the mysteries of the brain. However, identifying this circuitry
requires time-consuming, manual tracing (proofreading) due to the size and
intricacy of these image datasets, thus limiting state-of-the-art analysis to
very small brain regions. Potential avenues to improve scalability include
automatic image segmentation and crowd sourcing, but current efforts have had
limited success. In this paper, we propose a new strategy, focused
proofreading, that works with automatic segmentation and aims to limit
proofreading to the regions of a dataset that are most impactful to the
resulting circuit. We then introduce a novel workflow, which exploits
biological information such as synapses, and apply it to a large dataset in the
fly optic lobe. With our techniques, we achieve significant tracing speedups of
3-5x without sacrificing the quality of the resulting circuit. Furthermore, our
methodology makes the task of proofreading much more accessible and hence
potentially enhances the effectiveness of crowd sourcing
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