In the cerebral cortex, the activity levels of neuronal populations are continuously fluctuating. When neuronal activity, as measured using functional MRI (fMRI), is temporally coherent across 2 populations, those populations are said to be functionally connected. Functional connectivity has previously been shown to correlate with structural (anatomical) connectivity patterns at an aggregate level. In the present study we investigate, with the aid of computational modeling, whether systems-level properties of functional networks-including their spatial statistics and their persistence across time-can be accounted for by properties of the underlying anatomical network. We measured resting state functional connectivity (using fMRI) and structural connectivity (using diffusion spectrum imaging tractography) in the same individuals at high resolution. Structural connectivity then provided the couplings for a model of macroscopic cortical dynamics. In both model and data, we observed (i) that strong functional connections commonly exist between regions with no direct structural connection, rendering the inference of structural connectivity from functional connectivity impractical; (ii) that indirect connections and interregional distance accounted for some of the variance in functional connectivity that was unexplained by direct structural connectivity; and (iii) that resting-state functional connectivity exhibits variability within and across both scanning sessions and model runs. These empirical and modeling results demonstrate that although resting state functional connectivity is variable and is frequently present between regions without direct structural linkage, its strength, persistence, and spatial statistics are nevertheless constrained by the large-scale anatomical structure of the human cerebral cortex.computational model ͉ diffusion MRI ͉ neuroanatomy ͉ cerebral cortex ͉ brain networks P opulations of neurons in the mammalian cerebral cortex are continuously active during purposeful behavior, as well as during resting and sleep (1). Activity levels are modulated across time by the internal dynamics of each neuronal population and by signals received from cortical, subcortical, and peripheral elements of the nervous system. In the past decade, there has been intense interest in the patterns of correlated activity [''functional connectivity'' (2)] in the human brain, because these patterns are believed to reflect the patterns of interaction between neuronal populations. A set of functionally connected regions is referred to as a ''functional network.'' Some functional networks are most commonly detected when participants are not performing any demanding task (in the resting state); others are observed in the context of taskfocused behavior; and some networks persist across both behavioral states (3-6). A set of regions including posterior medial, anterior medial, and lateral parietal cortices comprise the default mode network (DMN) (7, 8), a functional network that is particularly robust across participants...

The active contour/snake model is one of the most successful variational models in image segmentation. It consists of evolving a contour in images toward the boundaries of objects. Its success is based on strong mathematical properties and efficient numerical schemes based on the level set method. The only drawback of this model is the existence of local minima in the active contour energy, which makes the initial guess critical to get satisfactory results. In this paper, we propose to solve this problem by determining a global minimum of the active contour model. Our approach is based on the unification of image segmentation and image denoising tasks into a global minimization framework. More precisely, we propose to unify three well-known image variational models, namely the snake model, the Rudin-Osher-Fatemi denoising model and the Mumford-Shah segmentation model. We will establish theorems with proofs to determine the existence of a global minimum of the active contour model. From a numerical point of view, we propose a new practical way to solve the active contour propagation problem toward object boundaries through a dual formulation of the minimization problem. The dual formulation, easy to implement, allows us a fast global minimization of the snake energy. It avoids the usual drawback in the level set approach that consists of initializing the active contour in a distance function and re-initializing it periodically during the evolution, which is time-consuming. We apply our segmentation algorithms on synthetic and real-world images, such as texture images and medical images, to emphasize the performances of our model compared with other segmentation models.

The complex relationship between structural and functional connectivity, as measured by noninvasive imaging of the human brain, poses many unresolved challenges and open questions. Here, we apply analytic measures of network communication to the structural connectivity of the human brain and explore the capacity of these measures to predict resting-state functional connectivity across three independently acquired datasets. We focus on the layout of shortest paths across the network and on two communication measures-search information and path transitivitywhich account for how these paths are embedded in the rest of the network. Search information is an existing measure of information needed to access or trace shortest paths; we introduce path transitivity to measure the density of local detours along the shortest path. We find that both search information and path transitivity predict the strength of functional connectivity among both connected and unconnected node pairs. They do so at levels that match or significantly exceed path length measures, Euclidean distance, as well as computational models of neural dynamics. This capacity suggests that dynamic couplings due to interactions among neural elements in brain networks are substantially influenced by the broader network context adjacent to the shortest communication pathways.connectome | graph theory | network theory | brain connectivity T he topology and dynamics of brain networks are a central focus of the emerging field of connectomics (1). A growing number of studies of human brain networks carried out with modern noninvasive neuroimaging methods have begun to characterize the architecture of structural networks (2-4), as well as spatially distributed components (5-7) and time-varying dynamics (8) of functional networks. Although structural connectivity (SC) is inferred from diffusion imaging and tractography, functional connectivity (FC) is generally derived from pairwise correlations of time series recorded during "resting" brain activity, measured with functional magnetic resonance imaging (fMRI). Both networks define a multiplex system (9) in which the SC level shapes or imposes constraints on the FC level. Indeed, mounting evidence indicates that SC and FC are robustly related. Numerous studies have documented strong and significant correlations between the strengths of structural and functional connections at whole-brain (2, 10-13) and mesoscopic scales (14), as well as acute changes in FC after perturbation of SC (15).Although there is ample evidence documenting statistical relationships between SC and FC, the causal role of SC in shaping whole-brain patterns of FC is still only incompletely understood. There are numerous reports of strong FC among brain regions that are not directly structurally connected, an effect that has been ascribed to signal propagation along one or more indirect structural paths (11), or to network-wide contextual influence (16). The present paper builds on two interrelated premises. First, if SC plays a major causal role...

From toddler to late teenager, the macroscopic pattern of axonal projections in the human brain remains largely unchanged while undergoing dramatic functional modifications that lead to network refinement. These functional modifications are mediated by increasing myelination and changes in axonal diameter and synaptic density, as well as changes in neurochemical mediators. Here we explore the contribution of white matter maturation to the development of connectivity between ages 2 and 18 y using high b-value diffusion MRI tractography and connectivity analysis. We measured changes in connection efficacy as the inverse of the average diffusivity along a fiber tract. We observed significant refinement in specific metrics of network topology, including a significant increase in node strength and efficiency along with a decrease in clustering. Major structural modules and hubs were in place by 2 y of age, and they continued to strengthen their profile during subsequent development. Recording resting-state functional MRI from a subset of subjects, we confirmed a positive correlation between structural and functional connectivity, and in addition observed that this relationship strengthened with age. Continuously increasing integration and decreasing segregation of structural connectivity with age suggests that network refinement mediated by white matter maturation promotes increased global efficiency. In addition, the strengthening of the correlation between structural and functional connectivity with age suggests that white matter connectivity in combination with other factors, such as differential modulation of axonal diameter and myelin thickness, that are partially captured by inverse average diffusivity, play an increasingly important role in creating brain-wide coherence and synchrony.connectome | development | graph | network dynamics | tractography M ost real-world networks do not arise all at once but, guided by rules, develop through a growth process that progressively fine-tunes the configuration of nodes and edges. Thus, an important aspect in the analysis of large-scale networks is the characterization of their dynamic development and evolution. From a theoretical point of view growth rules have been shown to have a significant effect on the emergent behavior of the final large-scale structural topology. For example, the emergence of scale-free networks can be explained by a preferential attachment rule (1, 2), with important functional consequences (3). If we can measure the growth and reshaping of connectivity that occurs with maturation during the developmental process, we can begin to infer growth rules governing this complex process and examine their functional consequences. These growth rules need to be instantiated in a biological system, and therefore the functional consequences would provide hypotheses linking emergent network properties to underlying cellular and molecular mechanisms.Real-world networks rarely grow according to simple statistical models, thus necessitating empirical sampling ov...