996 research outputs found
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
Evaluating 35 Methods to Generate Structural Connectomes Using Pairwise Classification
There is no consensus on how to construct structural brain networks from
diffusion MRI. How variations in pre-processing steps affect network
reliability and its ability to distinguish subjects remains opaque. In this
work, we address this issue by comparing 35 structural connectome-building
pipelines. We vary diffusion reconstruction models, tractography algorithms and
parcellations. Next, we classify structural connectome pairs as either
belonging to the same individual or not. Connectome weights and eight
topological derivative measures form our feature set. For experiments, we use
three test-retest datasets from the Consortium for Reliability and
Reproducibility (CoRR) comprised of a total of 105 individuals. We also compare
pairwise classification results to a commonly used parametric test-retest
measure, Intraclass Correlation Coefficient (ICC).Comment: Accepted for MICCAI 2017, 8 pages, 3 figure
Cytoskeletal changes during poliovirus infection in an intestinal cell line
Background and Objectives: Although polioviral replication has been extensively studied, cytoskeletal changes in the host cell during poliovirus replication have not been extensively investigated. We studied the ultrastructural and cytoskeletal changes in host cells during poliovirus infection. Methods: Fluorescence staining of filamentous actin with a fluorescein-isothiocynate labelled mycotoxin, in the absence and presence of microfilament inhibitors cytochalasins B and D, and electron microscopy were used to investigate the role and fate of actin microfilaments during poliovirus infection, morphogenesis and release in an intestinal cell line, HRT-18. Results: At 10 h post-infection, fluorescence staining of actin showed focal areas of fluorescence in the cytoplasm. By 16 h, these became more prominent and increased in number, and by 18-22 h they coalesced to enclose areas of the cytoplasm. These changes in the actin profile were confirmed by electron microscopy, where small actin bundles appeared in association with vesicles, increased in size, number and thickness, enclosed areas of cytoplasm with numerous vesicles and were finally seen in association with crystalline arrays of virus near the periphery of the cells. The addition of microfilament inhibitors cytochalasins B and D, after the initial period of adsorption resulted in complete inhibition of changes in the actin profile and of viral release, indicating that microfilament inhibitors prevented both polymerization of actin and movement of the virus within the cell. Interpretation and Conclusion: In poliovirus infection, both intracellular movement and release of virus appear to be related to cytoskeletal changes, particularly involving actin microfilaments
NETWORK FLOW WITH FUZZY ARC LENGTHS USING HAAR RANKING
ABSTRACT Shortest path problem is a classical and the most widely studied phenomenon in combinatorial optimization. In a classical shortest path problem, the distance of the arcs between different nodes of a network are assumed to be certain. In some uncertain situations, the distance will be calculated as a fuzzy number depending on the number of parameters considered. This article proposes a new approach based on Haar ranking of fuzzy numbers to find the shortest path between nodes of a given network. The combination of Haar ranking and the well-known Dijkstra's algorithm for finding the shortest path have been used to identify the shortest path between given nodes of a network. The numerical examples ensure the feasibility and validity of the proposed method
Cosmological models with bulk viscosity in presence of adiabatic matter creation and with G, c and Lambda variables
Some properties of cosmological models with a time variable bulk viscous
coefficient in presence of adiabatic mater creation and G, c, Lambda variables
are investigated in the framework of flat FRW line element. We trivially find a
set of solutions through Dimensional Analysis. In all the studied cases it is
found that the behaviour of these constants is inversely prportional to the
cosmic time.Comment: 12 pages. We have been rewriting and completing the bibliography of
this paper. Submitted to General Relativity and Gravitatio
Nonlinear spinor field in Bianchi type-I Universe filled with viscous fluid: numerical solutions
We consider a system of nonlinear spinor and a Bianchi type I gravitational
fields in presence of viscous fluid. The nonlinear term in the spinor field
Lagrangian is chosen to be , with being a self-coupling
constant and being a function of the invariants an constructed from
bilinear spinor forms and . Self-consistent solutions to the spinor and
BI gravitational field equations are obtained in terms of , where
is the volume scale of BI universe. System of equations for and \ve,
where \ve is the energy of the viscous fluid, is deduced. This system is
solved numerically for some special cases.Comment: 15 pages, 4 figure
Random walk centrality for temporal networks
Nodes can be ranked according to their relative importance within a network. Ranking algorithms based on random walks are particularly useful because they connect topological and diffusive properties of the network. Previous methods based on random walks, for example the PageRank, have focused on static structures. However, several realistic networks are indeed dynamic, meaning that their structure changes in time. In this paper, we propose a centrality measure for temporal networks based on random walks under periodic boundary conditions that we call TempoRank. It is known that, in static networks, the stationary density of the random walk is proportional to the degree or the strength of a node. In contrast, we find that, in temporal networks, the stationary density is proportional to the in-strength of the so-called effective network, a weighted and directed network explicitly constructed from the original sequence of transition matrices. The stationary density also depends on the sojourn probability q, which regulates the tendency of the walker to stay in the node, and on the temporal resolution of the data. We apply our method to human interaction networks and show that although it is important for a node to be connected to another node with many random walkers (one of the principles of the PageRank) at the right moment, this effect is negligible in practice when the time order of link activation is included
Squeeze-and-Breathe Evolutionary Monte Carlo Optimisation with Local Search Acceleration and its application to parameter fitting
Motivation: Estimating parameters from data is a key stage of the modelling
process, particularly in biological systems where many parameters need to be
estimated from sparse and noisy data sets. Over the years, a variety of
heuristics have been proposed to solve this complex optimisation problem, with
good results in some cases yet with limitations in the biological setting.
Results: In this work, we develop an algorithm for model parameter fitting
that combines ideas from evolutionary algorithms, sequential Monte Carlo and
direct search optimisation. Our method performs well even when the order of
magnitude and/or the range of the parameters is unknown. The method refines
iteratively a sequence of parameter distributions through local optimisation
combined with partial resampling from a historical prior defined over the
support of all previous iterations. We exemplify our method with biological
models using both simulated and real experimental data and estimate the
parameters efficiently even in the absence of a priori knowledge about the
parameters.Comment: 15 Pages, 3 Figures, 6 Tables; Availability: Matlab code available
from the authors upon reques
Nitric oxide sensing in plants is mediated by proteolytic control of group VII ERF transcription factors
Nitric oxide (NO) is an important signaling compound in prokaryotes and eukaryotes. In plants, NO regulates critical developmental transitions and stress responses. Here, we identify a mechanism for NO sensing that coordinates responses throughout development based on targeted degradation of plant-specific transcriptional regulators, the group VII ethylene response factors (ERFs). We show that the N-end rule pathway of targeted proteolysis targets these proteins for destruction in the presence of NO, and we establish them as critical regulators of diverse NO-regulated processes, including seed germination, stomatal closure, and hypocotyl elongation. Furthermore, we define the molecular mechanism for NO control of germination and crosstalk with abscisic acid (ABA) signaling through ERF-regulated expression of ABSCISIC ACID INSENSITIVE5 (ABI5). Our work demonstrates how NO sensing is integrated across multiple physiological processes by direct modulation of transcription factor stability and identifies group VII ERFs as central hubs for the perception of gaseous signals in plants
Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases
BACKGROUND: Clinical, pathological and genetic overlap between sporadic frontotemporal dementia (FTD), Alzheimer's disease (AD) and Parkinson's disease (PD) has been suggested; however, the relationship between these disorders is still not well understood. Here we evaluated genetic overlap between FTD, AD and PD to assess shared pathobiology and identify novel genetic variants associated with increased risk for FTD.
METHODS: Summary statistics were obtained from the International FTD Genomics Consortium, International PD Genetics Consortium and International Genomics of AD Project (n>75 000 cases and controls). We used conjunction false discovery rate (FDR) to evaluate genetic pleiotropy and conditional FDR to identify novel FTD-associated SNPs. Relevant variants were further evaluated for expression quantitative loci.
RESULTS: We observed SNPs within the HLA, MAPT and APOE regions jointly contributing to increased risk for FTD and AD or PD. By conditioning on polymorphisms associated with PD and AD, we found 11 loci associated with increased risk for FTD. Meta-analysis across two independent FTD cohorts revealed a genome-wide signal within the APOE region (rs6857, 3′-UTR=PVRL2, p=2.21×10–12), and a suggestive signal for rs1358071 within the MAPT region (intronic=CRHR1, p=4.91×10−7) with the effect allele tagging the H1 haplotype. Pleiotropic SNPs at the HLA and MAPT loci associated with expression changes in cis-genes supporting involvement of intracellular vesicular trafficking, immune response and endo/lysosomal processes.
CONCLUSIONS: Our findings demonstrate genetic pleiotropy in these neurodegenerative diseases and indicate that sporadic FTD is a polygenic disorder where multiple pleiotropic loci with small effects contribute to increased disease risk
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