7,784 research outputs found

    Suppressing decoherence and improving entanglement by quantum-jump-based feedback control in two-level systems

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    We study the quantum-jump-based feedback control on the entanglement shared between two qubits with one of them subject to decoherence, while the other qubit is under the control. This situation is very relevant to a quantum system consisting of nuclear and electron spins in solid states. The possibility to prolong the coherence time of the dissipative qubit is also explored. Numerical simulations show that the quantum-jump-based feedback control can improve the entanglement between the qubits and prolong the coherence time for the qubit subject directly to decoherence

    Patch-based Convolutional Neural Network for Whole Slide Tissue Image Classification

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    Convolutional Neural Networks (CNN) are state-of-the-art models for many image classification tasks. However, to recognize cancer subtypes automatically, training a CNN on gigapixel resolution Whole Slide Tissue Images (WSI) is currently computationally impossible. The differentiation of cancer subtypes is based on cellular-level visual features observed on image patch scale. Therefore, we argue that in this situation, training a patch-level classifier on image patches will perform better than or similar to an image-level classifier. The challenge becomes how to intelligently combine patch-level classification results and model the fact that not all patches will be discriminative. We propose to train a decision fusion model to aggregate patch-level predictions given by patch-level CNNs, which to the best of our knowledge has not been shown before. Furthermore, we formulate a novel Expectation-Maximization (EM) based method that automatically locates discriminative patches robustly by utilizing the spatial relationships of patches. We apply our method to the classification of glioma and non-small-cell lung carcinoma cases into subtypes. The classification accuracy of our method is similar to the inter-observer agreement between pathologists. Although it is impossible to train CNNs on WSIs, we experimentally demonstrate using a comparable non-cancer dataset of smaller images that a patch-based CNN can outperform an image-based CNN

    Saran Wrap Handling Device

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    q-deformed Supersymmetric t-J Model with a Boundary

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    The q-deformed supersymmetric t-J model on a semi-infinite lattice is diagonalized by using the level-one vertex operators of the quantum affine superalgebra Uq[sl(2∣1)^]U_q[\hat{sl(2|1)}]. We give the bosonization of the boundary states. We give an integral expression of the correlation functions of the boundary model, and derive the difference equations which they satisfy.Comment: LaTex file 18 page

    Probing flavor changing interactions in hadron collisions

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    The subprocess gg→tcˉ+tˉcgg \to t\bar{c}+\bar{t}c in the two-Higgs-doublet model with flavor-changing scalar couplings is examined at the one loop level. With perturbative QCD factorization theorem, the corresponding cross sections for hadron-hadron collisions are computed numerically. The results are applicable to the whole mass range of the weakly coupled Higgs bosons. In case we could efficiently exclude the severe backgrounds of the tcˉ(tˉc)t\bar{c}(\bar{t}c) production signal, probing the flavor-changing top-charm-scalar vertex at hadron colliders would be very promising and accessible experimentally.Comment: LaTex file, 14 pages, 8 EPS figure

    Impact of Cross-Ancestry Genetic Architecture on GWASS in Admixed Populations

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    Genome-wide association studies (GWASs) have identified thousands of variants for disease risk. These studies have predominantly been conducted in individuals of European ancestries, which raises questions about their transferability to individuals of other ancestries. Of particular interest are admixed populations, usually defined as populations with recent ancestry from two or more continental sources. Admixed genomes contain segments of distinct ancestries that vary in composition across individuals in the population, allowing for the same allele to induce risk for disease on different ancestral backgrounds. This mosaicism raises unique challenges for GWASs in admixed populations, such as the need to correctly adjust for population stratification. In this work we quantify the impact of differences in estimated allelic effect sizes for risk variants between ancestry backgrounds on association statistics. Specifically, while the possibility of estimated allelic effect-size heterogeneity by ancestry (HetLanc) can be modeled when performing a GWAS in admixed populations, the extent of HetLanc needed to overcome the penalty from an additional degree of freedom in the association statistic has not been thoroughly quantified. Using extensive simulations of admixed genotypes and phenotypes, we find that controlling for and conditioning effect sizes on local ancestry can reduce statistical power by up to 72%. This finding is especially pronounced in the presence of allele frequency differentiation. We replicate simulation results using 4,327 African-European admixed genomes from the UK Biobank for 12 traits to find that for most significant SNPs, HetLanc is not large enough for GWASs to benefit from modeling heterogeneity in this way
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