65,697 research outputs found
Towards a Multi-Subject Analysis of Neural Connectivity
Directed acyclic graphs (DAGs) and associated probability models are widely
used to model neural connectivity and communication channels. In many
experiments, data are collected from multiple subjects whose connectivities may
differ but are likely to share many features. In such circumstances it is
natural to leverage similarity between subjects to improve statistical
efficiency. The first exact algorithm for estimation of multiple related DAGs
was recently proposed by Oates et al. 2014; in this letter we present examples
and discuss implications of the methodology as applied to the analysis of fMRI
data from a multi-subject experiment. Elicitation of tuning parameters requires
care and we illustrate how this may proceed retrospectively based on technical
replicate data. In addition to joint learning of subject-specific connectivity,
we allow for heterogeneous collections of subjects and simultaneously estimate
relationships between the subjects themselves. This letter aims to highlight
the potential for exact estimation in the multi-subject setting.Comment: to appear in Neural Computation 27:1-2
Size Control in the Nanoprecipitation Process of Stable Iodine (127I) Using Microchannel Reactor—Optimization by Artificial Neural Networks
In this study, nanosuspension of stable iodine (127I) was prepared by nanoprecipitation process in microfluidic devices. Then, size of particles was optimized using artificial neural networks (ANNs) modeling. The size of prepared particles was evaluated by dynamic light scattering. The response surfaces obtained from ANNs model illustrated the determining effect of input variables (solvent and antisolvent flow rate, surfactant concentration, and solvent temperature) on the output variable (nanoparticle size). Comparing the 3D graphs revealed that solvent and antisolvent flow rate had reverse relation with size of nanoparticles. Also, those graphs indicated that the solvent temperature at low values had an indirect relation with size of stable iodine (127I) nanoparticles, while at the high values, a direct relation was observed. In addition, it was found that the effect of surfactant concentration on particle size in the nanosuspension of stable iodine (127I) was depended on the solvent temperature. © 2015, American Association of Pharmaceutical Scientists
Neural Substrates of Chronic Pain in the Thalamocortical Circuit
Chronic pain (CP), a pathological condition with a large repertory of signs and symptoms, has no recognizable neural functional common hallmark shared by its diverse expressions. The aim of the present research was to identify potential dynamic markers shared in CP models, by using simultaneous electrophysiological extracellular recordings from the rat ventrobasal thalamus and the primary somatosensory cortex. We have been able to extract a neural signature attributable solely to CP, independent from of the originating conditions. This study showed disrupted functional connectivity and increased redundancy in firing patterns in CP models versus controls, and interpreted these signs as a neural signature of CP. In a clinical perspective, we envisage CP as disconnection syndrome and hypothesize potential novel therapeutic appraisal
Shift Aggregate Extract Networks
We introduce an architecture based on deep hierarchical decompositions to
learn effective representations of large graphs. Our framework extends classic
R-decompositions used in kernel methods, enabling nested "part-of-part"
relations. Unlike recursive neural networks, which unroll a template on input
graphs directly, we unroll a neural network template over the decomposition
hierarchy, allowing us to deal with the high degree variability that typically
characterize social network graphs. Deep hierarchical decompositions are also
amenable to domain compression, a technique that reduces both space and time
complexity by exploiting symmetries. We show empirically that our approach is
competitive with current state-of-the-art graph classification methods,
particularly when dealing with social network datasets
Learning to Discover Sparse Graphical Models
We consider structure discovery of undirected graphical models from
observational data. Inferring likely structures from few examples is a complex
task often requiring the formulation of priors and sophisticated inference
procedures. Popular methods rely on estimating a penalized maximum likelihood
of the precision matrix. However, in these approaches structure recovery is an
indirect consequence of the data-fit term, the penalty can be difficult to
adapt for domain-specific knowledge, and the inference is computationally
demanding. By contrast, it may be easier to generate training samples of data
that arise from graphs with the desired structure properties. We propose here
to leverage this latter source of information as training data to learn a
function, parametrized by a neural network that maps empirical covariance
matrices to estimated graph structures. Learning this function brings two
benefits: it implicitly models the desired structure or sparsity properties to
form suitable priors, and it can be tailored to the specific problem of edge
structure discovery, rather than maximizing data likelihood. Applying this
framework, we find our learnable graph-discovery method trained on synthetic
data generalizes well: identifying relevant edges in both synthetic and real
data, completely unknown at training time. We find that on genetics, brain
imaging, and simulation data we obtain performance generally superior to
analytical methods
Disentangling causal webs in the brain using functional Magnetic Resonance Imaging: A review of current approaches
In the past two decades, functional Magnetic Resonance Imaging has been used
to relate neuronal network activity to cognitive processing and behaviour.
Recently this approach has been augmented by algorithms that allow us to infer
causal links between component populations of neuronal networks. Multiple
inference procedures have been proposed to approach this research question but
so far, each method has limitations when it comes to establishing whole-brain
connectivity patterns. In this work, we discuss eight ways to infer causality
in fMRI research: Bayesian Nets, Dynamical Causal Modelling, Granger Causality,
Likelihood Ratios, LiNGAM, Patel's Tau, Structural Equation Modelling, and
Transfer Entropy. We finish with formulating some recommendations for the
future directions in this area
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