22,564 research outputs found
Development of a Bidirectional Pedestrian Stream Model with an Oblique Intersecting Angle
This paper establishes a mathematical model that can represent the conflicting effects of two pedestrian streams that have an oblique intersecting angle in a large crowd. In a previous paper, a controlled experiment in which two streams of pedestrians were asked to walk in designated directions was used to model the bidirectional pedestrian stream of certain intersecting angles. In this paper, the writers revisit that problem and apply the Bayesian inference method to calibrate an improved model with the controlled experiment data. Pedestrian movement data are also collected from a busy crosswalk by using a video observation approach. The two sets of data are used separately to calibrate the proposed model. With the calibrated model, the relationship between speed, density, and flow is studied in both the reference and conflicting streams, and a prediction is made regarding how these factors affected the interactions of moving pedestrian streams. It is found that the speed of one stream not only decreases with its total density, but also decreases with the ratio of its flow relative to the total flow, i.e., the speed of the pedestrians decreases if their stream changes from the major to minor stream. It is also observed that the maximum disruption that was induced by pedestrian flow from an intersecting angle occurs when the angle is approximately 135°.postprin
Selection bias in build-operate-transfer transportation project appraisals
Recent empirical studies have found widespread inaccuracies in traffic forecasts despite the fact that travel demand forecasting models have been significantly improved over the past few decades. We suspect that an intrinsic selection bias may exist in the competitive project appraisal process, in addition to the many other factors that contribute to inaccurate traffic forecasts. In this paper, we examine the potential for selection bias in the governmental process of Build-Operate-Transfer (BOT) transportation project appraisals. Although the simultaneous consideration of multiple criteria is typically used in practice, traffic flow estimate is usually a key criterion in these appraisals. For the purposes of this paper, we focus on the selection bias associated with the highest flow estimate criterion. We develop two approaches to quantify the level and chance of inaccuracy caused by selection bias: the expected value approach and the probability approach. The expected value approach addresses the question “to what extent is inaccuracy caused by selection bias?”. The probability approach addresses the question “what is the chance of inaccuracy due to selection bias?”. The results of this analysis confirm the existence of selection bias when a government uses the highest traffic forecast estimate as the priority criterion for BOT project selection. In addition, we offer some insights into the relationship between the extent/chance of inaccuracy and other related factors. We do not argue that selection bias is the only reason for inaccurate traffic forecasts in BOT projects; however, it does appear that it could be an intrinsic factor worthy of further attention and investigation.postprin
Multiplicative random walk Metropolis-Hastings on the real line
In this article we propose multiplication based random walk Metropolis
Hastings (MH) algorithm on the real line. We call it the random dive MH (RDMH)
algorithm. This algorithm, even if simple to apply, was not studied earlier in
Markov chain Monte Carlo literature. The associated kernel is shown to have
standard properties like irreducibility, aperiodicity and Harris recurrence
under some mild assumptions. These ensure basic convergence (ergodicity) of the
kernel. Further the kernel is shown to be geometric ergodic for a large class
of target densities on . This class even contains realistic target
densities for which random walk or Langevin MH are not geometrically ergodic.
Three simulation studies are given to demonstrate the mixing property and
superiority of RDMH to standard MH algorithms on real line. A share-price
return data is also analyzed and the results are compared with those available
in the literature
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
Understanding the genetic factors underlying neurodevelopmental and neuropsychiatric disorders is a major challenge given their prevalence and potential severity for quality of life. While large-scale genomic screens have made major advances in this area, for many disorders the genetic underpinnings are complex and poorly understood. To date the field has focused predominantly on protein coding variation, but given the importance of tightly controlled gene expression for normal brain development and disorder, variation that affects non-coding regulatory regions of the genome is likely to play an important role in these phenotypes. Herein we show the importance of 3 prime untranslated region (3'UTR) non-coding regulatory variants across neurodevelopmental and neuropsychiatric disorders. We devised a pipeline for identifying and functionally validating putatively pathogenic variants from next generation sequencing (NGS) data. We applied this pipeline to a cohort of children with severe specific language impairment (SLI) and identified a functional, SLI-associated variant affecting gene regulation in cells and post-mortem human brain. This variant and the affected gene (ARHGEF39) represent new putative risk factors for SLI. Furthermore, we identified 3'UTR regulatory variants across autism, schizophrenia and bipolar disorder NGS cohorts demonstrating their impact on neurodevelopmental and neuropsychiatric disorders. Our findings show the importance of investigating non-coding regulatory variants when determining risk factors contributing to neurodevelopmental and neuropsychiatric disorders. In the future, integration of such regulatory variation with protein coding changes will be essential for uncovering the genetic causes of complex neurological disorders and the fundamental mechanisms underlying health and disease
Parameter Estimation and Quantitative Parametric Linkage Analysis with GENEHUNTER-QMOD
Objective: We present a parametric method for linkage analysis of quantitative phenotypes. The method provides a test for linkage as well as an estimate of different phenotype parameters. We have implemented our new method in the program GENEHUNTER-QMOD and evaluated its properties by performing simulations. Methods: The phenotype is modeled as a normally distributed variable, with a separate distribution for each genotype. Parameter estimates are obtained by maximizing the LOD score over the normal distribution parameters with a gradient-based optimization called PGRAD method. Results: The PGRAD method has lower power to detect linkage than the variance components analysis (VCA) in case of a normal distribution and small pedigrees. However, it outperforms the VCA and Haseman-Elston regression for extended pedigrees, nonrandomly ascertained data and non-normally distributed phenotypes. Here, the higher power even goes along with conservativeness, while the VCA has an inflated type I error. Parameter estimation tends to underestimate residual variances but performs better for expectation values of the phenotype distributions. Conclusion: With GENEHUNTER-QMOD, a powerful new tool is provided to explicitly model quantitative phenotypes in the context of linkage analysis. It is freely available at http://www.helmholtz-muenchen.de/genepi/downloads. Copyright (C) 2012 S. Karger AG, Base
Science Models as Value-Added Services for Scholarly Information Systems
The paper introduces scholarly Information Retrieval (IR) as a further
dimension that should be considered in the science modeling debate. The IR use
case is seen as a validation model of the adequacy of science models in
representing and predicting structure and dynamics in science. Particular
conceptualizations of scholarly activity and structures in science are used as
value-added search services to improve retrieval quality: a co-word model
depicting the cognitive structure of a field (used for query expansion), the
Bradford law of information concentration, and a model of co-authorship
networks (both used for re-ranking search results). An evaluation of the
retrieval quality when science model driven services are used turned out that
the models proposed actually provide beneficial effects to retrieval quality.
From an IR perspective, the models studied are therefore verified as expressive
conceptualizations of central phenomena in science. Thus, it could be shown
that the IR perspective can significantly contribute to a better understanding
of scholarly structures and activities.Comment: 26 pages, to appear in Scientometric
What has finite element analysis taught us about diabetic foot disease and its management?:a systematic review
Over the past two decades finite element (FE) analysis has become a popular tool for researchers seeking to simulate the biomechanics of the healthy and diabetic foot. The primary aims of these simulations have been to improve our understanding of the foot's complicated mechanical loading in health and disease and to inform interventions designed to prevent plantar ulceration, a major complication of diabetes. This article provides a systematic review and summary of the findings from FE analysis-based computational simulations of the diabetic foot.A systematic literature search was carried out and 31 relevant articles were identified covering three primary themes: methodological aspects relevant to modelling the diabetic foot; investigations of the pathomechanics of the diabetic foot; and simulation-based design of interventions to reduce ulceration risk.Methodological studies illustrated appropriate use of FE analysis for simulation of foot mechanics, incorporating nonlinear tissue mechanics, contact and rigid body movements. FE studies of pathomechanics have provided estimates of internal soft tissue stresses, and suggest that such stresses may often be considerably larger than those measured at the plantar surface and are proportionally greater in the diabetic foot compared to controls. FE analysis allowed evaluation of insole performance and development of new insole designs, footwear and corrective surgery to effectively provide intervention strategies. The technique also presents the opportunity to simulate the effect of changes associated with the diabetic foot on non-mechanical factors such as blood supply to local tissues.While significant advancement in diabetic foot research has been made possible by the use of FE analysis, translational utility of this powerful tool for routine clinical care at the patient level requires adoption of cost-effective (both in terms of labour and computation) and reliable approaches with clear clinical validity for decision making
Self-assembly of Microcapsules via Colloidal Bond Hybridization and Anisotropy
Particles with directional interactions are promising building blocks for new
functional materials and may serve as models for biological structures.
Mutually attractive nanoparticles that are deformable due to flexible surface
groups, for example, may spontaneously order themselves into strings, sheets
and large vesicles. Furthermore, anisotropic colloids with attractive patches
can self-assemble into open lattices and colloidal equivalents of molecules and
micelles. However, model systems that combine mutual attraction, anisotropy,
and deformability have---to the best of our knowledge---not been realized.
Here, we synthesize colloidal particles that combine these three
characteristics and obtain self-assembled microcapsules. We propose that mutual
attraction and deformability induce directional interactions via colloidal bond
hybridization. Our particles contain both mutually attractive and repulsive
surface groups that are flexible. Analogous to the simplest chemical bond,
where two isotropic orbitals hybridize into the molecular orbital of H2, these
flexible groups redistribute upon binding. Via colloidal bond hybridization,
isotropic spheres self-assemble into planar monolayers, while anisotropic
snowman-like particles self-assemble into hollow monolayer microcapsules. A
modest change of the building blocks thus results in a significant leap in the
complexity of the self-assembled structures. In other words, these relatively
simple building blocks self-assemble into dramatically more complex structures
than similar particles that are isotropic or non-deformable
Differential expression analysis with global network adjustment
<p>Background: Large-scale chromosomal deletions or other non-specific perturbations of the transcriptome can alter the expression of hundreds or thousands of genes, and it is of biological interest to understand which genes are most profoundly affected. We present a method for predicting a gene’s expression as a function of other genes thereby accounting for the effect of transcriptional regulation that confounds the identification of genes differentially expressed relative to a regulatory network. The challenge in constructing such models is that the number of possible regulator transcripts within a global network is on the order of thousands, and the number of biological samples is typically on the order of 10. Nevertheless, there are large gene expression databases that can be used to construct networks that could be helpful in modeling transcriptional regulation in smaller experiments.</p>
<p>Results: We demonstrate a type of penalized regression model that can be estimated from large gene expression databases, and then applied to smaller experiments. The ridge parameter is selected by minimizing the cross-validation error of the predictions in the independent out-sample. This tends to increase the model stability and leads to a much greater degree of parameter shrinkage, but the resulting biased estimation is mitigated by a second round of regression. Nevertheless, the proposed computationally efficient “over-shrinkage” method outperforms previously used LASSO-based techniques. In two independent datasets, we find that the median proportion of explained variability in expression is approximately 25%, and this results in a substantial increase in the signal-to-noise ratio allowing more powerful inferences on differential gene expression leading to biologically intuitive findings. We also show that a large proportion of gene dependencies are conditional on the biological state, which would be impossible with standard differential expression methods.</p>
<p>Conclusions: By adjusting for the effects of the global network on individual genes, both the sensitivity and reliability of differential expression measures are greatly improved.</p>
Structure-based enzyme engineering improves donor-substrate recognition of Arabidopsis thaliana Glycosyltransferases
Glycosylation of secondary metabolites involves plant UDP-dependent glycosyltransferases (UGTs). UGTs have shown promise as catalysts in the synthesis of glycosides for medical treatment. However, limited understanding at the molecular level due to insufficient biochemical and structural information has hindered potential applications of most of these UGTs. In the absence of experimental crystal structures, we employed advanced molecular modelling and simulations in conjunction with biochemical characterisation to design a workflow to study five Group H Arabidopsis thaliana (76E1, 76E2, 76E4, 76E5, 76D1) UGTs. Based on our rational structural manipulation and analysis, we identified key amino acids (P129 in 76D1; D374 in 76E2; K275 in 76E4), which when mutated improved donor-substrate recognition than wildtype UGTs. Molecular dynamics simulations and deep learning analysis identified structural differences, which drive substrate preferences. The design of these UGTs with broader substrate specificity may play important role in biotechnological and industrial applications. These findings can also serve as basis to study other plant UGTs and thereby advancing UGT enzyme engineering.Federal Scholarship Board/Presidential Special Scholarship Scheme for Innovation and Development (PRESSID), Nigeria; Sichuan Science and Technology Progra
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