6,733 research outputs found

    A Comparison Between Stochastic and Deterministic Models of a Biological Oscillator

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    We look at the behavior of biological oscillators, specifically analyzing a genetic circuit that has oscillatory behavior. Implementing the system in deterministic and stochastic models, we compare the two models using various tests and analyze the effect of stochastic noise on these oscillations. We first investigate the effect of volume and find that at small system volumes, stochastic events cause the system to exhibit more sporadic oscillations and a longer period of oscillation. Next, we develop classification systems for discerning the boundary in the parameter space where the model begins to show oscillations. This is more challenging in the stochastic model, due to persistent fluctuations. We compare different methods of analysis of our deterministic and stochastic models and visualize the conditions which lead to oscillation in each model. We find that the parameter range of oscillation is larger in the stochastic model than in the deterministic model. Finally, we find an increased rate of mRNA production can create greater noise in a system and amplify the difference between a stochastic and deterministic system

    Significant cross-species gene flow detected in the Tamias quadrivittatus group of North American chipmunks

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    In the past two decades genomic data have been widely used to detect historical gene flow between species in a variety of plants and animals. The Tamias quadrivittatus group of North America chipmunks, which originated through a series of rapid speciation events, are known to undergo massive amounts of mitochondrial introgression. Yet in a recent analysis of targeted nuclear loci from the group, no evidence for cross-species introgression was detected, indicating widespread cytonuclear discordance. The study used heuristic methods that analyze summaries of the multilocus sequence data to detect gene flow, which may suffer from low power. Here we use the full likelihood method implemented in the Bayesian program BPP to reanalyze these data. We take a stepwise approach to constructing an introgression model by adding introgression events onto a well-supported binary species tree. The analysis detected robust evidence for multiple ancient introgression events affecting the nuclear genome, with introgression probabilities reaching 65%. We estimate population parameters and highlight the fact that species divergence times may be seriously underestimated if ancient cross-species gene flow is ignored in the analysis. Our analyses highlight the importance of using adequate statistical methods to reach reliable biological conclusions concerning cross-species gene flow

    Power of Bayesian and heuristic tests to detect cross-species introgression with reference to gene flow in the Tamias quadrivittatus group of North American chipmunks

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    In the past two decades genomic data have been widely used to detect historical gene flow between species in a variety of plants and animals. The Tamias quadrivittatus group of North America chipmunks, which originated through a series of rapid speciation events, are known to undergo massive amounts of mitochondrial introgression. Yet in a recent analysis of targeted nuclear loci from the group, no evidence for cross-species introgression was detected, indicating widespread cytonuclear discordance. The study used the heuristic method HyDe to detect gene flow, which may suffer from low power. Here we use the Bayesian method implemented in the program bpp to reanalyze these data. We develop a Bayesian test of introgression, calculating the Bayes factor via the Savage-Dickey density ratio using the Markov chain Monte Carlo (MCMC) sample under the model of introgression. We take a stepwise approach to constructing an introgression model by adding introgression events onto a well-supported binary species tree. The analysis detected robust evidence for multiple ancient introgression events affecting the nuclear genome, with introgression probabilities reaching 63%. We estimate population parameters and highlight the fact that species divergence times may be seriously underestimated if ancient cross-species gene flow is ignored in the analysis. We examine the assumptions and performance of HyDe, and demonstrate that it lacks power if gene flow occurs between sister lineages or if the mode of gene flow does not match the assumed hybrid speciation model with symmetrical population sizes. Our analyses highlight the power of likelihood-based inference of cross-species gene flow using genomic sequence data

    Heavy-quark contribution to the proton's magnetic moment

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    We study the contribution to the proton's magnetic moment from a heavy quark sea in quantum chromodynamics. The heavy quark is integrated out perturbatively to obtain an effective dimension-6 magnetic moment operator composed of three gluon fields. The leading contribution to the matrix element in the proton comes from a quadratically divergent term associated with a light-quark tensor operator. With an approximate knowledge of the proton's tensor charge, we conclude that a heavy sea-quark contribution to the proton's magnetic moment is positive in the asymptotic limit. We comment on the implication of this result for the physical strange quark.Comment: 4 pages, 2 figure

    Three-Quark Light-Cone Amplitudes of The Proton And Quark-Orbital-Motion Dependent Observables

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    We study the three-quark light-cone amplitudes of the proton including quarks' transverse momenta. We classify these amplitudes using a newly-developed method in which light-cone wave functions are constructed from a class of light-cone matrix elements. We derive the constraints on the amplitudes from parity and time-reversal symmetries. We use the amplitudes to calculate the physical observables which vanish when the quark orbital angular momentum is absent. These include transverse-momentum dependent parton distributions ΔqT(x,k)\Delta q_T(x, k_\perp), qT(x,k)q_T(x, k_\perp), δq(x,k)\delta q(x, k_\perp), and δqL(x,k)\delta q_L(x,k_\perp), twist-three parton distributions gT(x)g_T(x) and hL(x)h_L(x), helicity-flip generalized parton distributions E(x,ξ=0,Q2)E(x, \xi=0, Q^2) and its associates, and the Pauli form factor F2(Q2)F_2(Q^2).Comment: 20 pages, no figur

    An Analysis of the Next-to-Leading Order Corrections to the g_T(=g_1+g_2) Scaling Function

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    We present a general method for obtaining the quantum chromodynamical radiative corrections to the higher-twist (power-suppressed) contributions to inclusive deep-inelastic scattering in terms of light-cone correlation functions of the fundamental fields of quantum chromodynamics. Using this procedure, we calculate the previously unknown O(αs){\cal O}(\alpha_s) corrections to the twist-three part of the spin scaling function gT(xB,Q2)(=g1(xB,Q2)+g2(xB,Q2))g_T(x_B,Q^2) (=g_1(x_B,Q^2)+g_2(x_B,Q^2)) and the corresponding forward Compton amplitude ST(ν,Q2)S_T(\nu,Q^2). Expanding our result about the unphysical point xB=x_B=\infty, we arrive at an operator product expansion of the nonlocal product of two electromagnetic current operators involving twist-two and -three operators valid to O(αs){\cal O}(\alpha_s) for forward matrix elements. We find that the Wandzura-Wilczek relation between g1(xB,Q2)g_1(x_B,Q^2) and the twist-two part of gT(xB,Q2)g_T(x_B,Q^2) is respected in both the singlet and non-singlet sectors at this order, and argue its validity to all orders. The large-NcN_c limit does not appreciably simplify the twist-three Wilson coefficients.Comment: 41 pages, 9 figures, corrected minor erro

    PCD13: PATIENT BENEFIT QUESTIONNAIRE (PBQ) FOR XEROSTOMIA: DEVELOPMENT AND VALIDATION REPORT

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    Exclusive production of lepton, quark and meson pairs in peripheral ultrarelativistic heavy ion collisions

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    We discuss exclusive production of lepton-antilepton, quark-antiquark, ππ\pi \pi and ρ0ρ0\rho^0 \rho^0 pairs in ultraperipheral, ultrarelativistic heavy-ion collisions. The cross sections for exclusive production of pairs of particles is calculated in Equivalent Photon Approximation (EPA). Realistic (Fourier transform of charge density) charge form factors of nuclei are used and the corresponding results are compared with the cross sections calculated with monopole form factor used in the literature. Absorption effects are discussed and quantified. The cross sections obtained with realistic form factors are significantly smaller than those obtained with the monopole form factors.Comment: 9 pages, 13 figures an invited talk at the international conference "Hadron Structure 2011", Slovakia, June 201
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