691 research outputs found

    Isospin effects on the energy of vanishing flow in heavy-ion collisions

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    Using the isospin-dependent quantum molecular dynamics model we study the isospin effects on the disappearance of flow for the reactions of 58Ni^{58}Ni + 58Ni^{58}Ni and 58Fe^{58}Fe +58Fe^{58}Fe as a function of impact parameter. We found good agreement between our calculations and experimentally measured energy of vanishing flow at all colliding geometries. Our calculations reproduce the experimental data within 5%(10%) at central (peripheral) geometries

    Antimicrobial sensitivity pattern of gram positive CSF isolates in children with septic meningitis in a Tertiary Care Hospital

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    The present study was conducted with the objective to determineantimicrobial susceptibility of Gram positive CSF isolates in septic meningitis in a tertiary care hospital. CSF (3-5 ml) was collected from 638 admitted children clinically suspected of septic meningitis. Bacterial isolates were identified and microbial sensitivity was assessed by the Kirby-Bauer’s disk diffusion method. Of the samples tested 102 (15.99%) were culture positive of which 45 (44.12%) culture positives were found inchildren aged 1-12 years. M: F ratio was 1.62:1. Maximum incidence (51 cases) was in summer-rainy season and in institutional delivery (58 cases). Primary immunization did not protect against septic meningitis. The isolates in 66 (64.71%) cases were Gram positive of which 36 (54.55%) were Streptococcus spp., 24 (36.36%) Staphylococcus aureus and 6 (9.09%) cases coagulase negative Staphylococcus (CONS). Both Streptococci and coagulase negative Staphylococci were highly sensitive (100%) to Linezolid, Vancomycin and Piperacillin-Tazobactam. However, Staphylococcus aureus were 100% sensitive to Linezolid and Vancomycin but were only 87.5% sensitive to Piperacillin-Tazobactam combination. The Streptococcus species showed a high degree of resistance to Tetracyclin91.67%, Co-trimoxazole 88.89% and Penicillin 63.89%. Staphylococcus aureus showed resistance to the tune of 83.33% each to Tetracycline and Co-trimoxazxole and 79.17% with Penicillin. In case of coagulase negative Staphylococcus, Co-trimoxazole showed resistance in 83.33%, Penicillin in 66.67% and Tetracycline in 50% cases. In septic meningitis Gram positive isolates predominate. Therapy should be based on trends of bacterial sensitivity

    Editable AI: Mixed Human-AI Authoring of Code Patterns

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    Developers authoring HTML documents define elements following patterns which establish and reflect the visual structure of a document, such as making all images in a footer the same height by applying a class to each. To surface these patterns to developers and support developers in authoring consistent with these patterns, we propose a mixed human-AI technique for creating code patterns. Patterns are first learned from individual HTML documents through a decision tree, generating a representation which developers may view and edit. Code patterns are used to offer developers autocomplete suggestions, list examples, and flag violations. To evaluate our technique, we conducted a user study in which 24 participants wrote, edited, and corrected HTML documents. We found that our technique enabled developers to edit and correct documents more quickly and create, edit, and correct documents more successfully

    Kaposi's sarcoma-associated herpesvirus oncoprotein K13 protects against B cell receptor induced growth arrest and apoptosis through NF-κB activation

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    Kaposi's sarcoma-associated herpesvirus (KSHV) has been linked to the development of Kaposi's sarcoma, primary effusion lymphoma and multicentric Castleman's disease (MCD). We have characterized the role of KSHV-encoded viral FLICE inhibitory protein K13 in the modulation of anti-IgM induced growth arrest and apoptosis in B cells. We demonstrate that K13 protects WEHI 231, an immature B cell line, against anti-IgM induced growth arrest and apoptosis. The protective effect of K13 was associated with the activation of the NF-κB pathway and was deficient in its mutant, K13-58AAA, and a structural homolog, vFLIP E8, which lack NF-κB activity. K13 upregulated the expression of NF-κB subunit RelB and blocked the anti-IgM induced decline in c-Myc and rise in p27(Kip1) that have been associated with growth arrest and apoptosis. K13 also upregulated the expression of Mcl-1, an anti-apoptotic member of the Bcl2 family. Finally, K13 protected the mature B cell line Ramos against anti-IgM induced apoptosis through NF-κB activation. Inhibition of anti-IgM induced apoptosis by K13 may contribute to the development of KSHV-associated lymphoproliferative disorders

    Rapid, ultra low coverage copy number profiling of cell-free DNA as a precision oncology screening strategy.

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    Current cell-free DNA (cfDNA) next generation sequencing (NGS) precision oncology workflows are typically limited to targeted and/or disease-specific applications. In advanced cancer, disease burden and cfDNA tumor content are often elevated, yielding unique precision oncology opportunities. We sought to demonstrate the utility of a pan-cancer, rapid, inexpensive, whole genome NGS of cfDNA approach (PRINCe) as a precision oncology screening strategy via ultra-low coverage (~0.01x) tumor content determination through genome-wide copy number alteration (CNA) profiling. We applied PRINCe to a retrospective cohort of 124 cfDNA samples from 100 patients with advanced cancers, including 76 men with metastatic castration-resistant prostate cancer (mCRPC), enabling cfDNA tumor content approximation and actionable focal CNA detection, while facilitating concordance analyses between cfDNA and tissue-based NGS profiles and assessment of cfDNA alteration associations with mCRPC treatment outcomes. Therapeutically relevant focal CNAs were present in 42 (34%) cfDNA samples, including 36 of 93 (39%) mCRPC patient samples harboring AR amplification. PRINCe identified pre-treatment cfDNA CNA profiles facilitating disease monitoring. Combining PRINCe with routine targeted NGS of cfDNA enabled mutation and CNA assessment with coverages tuned to cfDNA tumor content. In mCRPC, genome-wide PRINCe cfDNA and matched tissue CNA profiles showed high concordance (median Pearson correlation = 0.87), and PRINCe detectable AR amplifications predicted reduced time on therapy, independent of therapy type (Kaplan-Meier log-rank test, chi-square = 24.9, p < 0.0001). Our screening approach enables robust, broadly applicable cfDNA-based precision oncology for patients with advanced cancer through scalable identification of therapeutically relevant CNAs and pre-/post-treatment genomic profiles, enabling cfDNA- or tissue-based precision oncology workflow optimization

    Successful management of aggressive fibromatosis of the neck using wide surgical excision: a case report

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    <p>Abstract</p> <p>Introduction</p> <p>Aggressive fibromatosis is a benign tumor, thought to arise from deep musculoaponeurotic structures, rarely found in the head or neck. However, when it does occur in the head and neck region, it tends to be more aggressive and associated with significant morbidity, which may be attributed to the vital vascular, neurological or anatomical structures in close proximity.</p> <p>Case presentation</p> <p>We report the case of a 39-year-old Pakistani man who presented with a two-month history of a lump on the right side of his neck. The mass was excised and histopathological analysis revealed a case of aggressive fibromatosis.</p> <p>Conclusion</p> <p>Due to the rarity of the condition no guidelines are available on the indications and extent of each modality. Due to its aggressive behavior and tendency to invade local structures and recur, a multi-modality management strategy is usually employed. On the basis of this case, we suggest that aggressive surgery is a viable management option and may be successfully used as a single modality treatment.</p

    Trading-off Data Fit and Complexity in Training Gaussian Processes with Multiple Kernels

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    This is the author accepted manuscript. The final version is available from Springer Verlag via the DOI in this recordLOD 2019: Fifth International Conference on Machine Learning, Optimization, and Data Science, 10-13 September 2019, Siena, ItalyGaussian processes (GPs) belong to a class of probabilistic techniques that have been successfully used in different domains of machine learning and optimization. They are popular because they provide uncertainties in predictions, which sets them apart from other modelling methods providing only point predictions. The uncertainty is particularly useful for decision making as we can gauge how reliable a prediction is. One of the fundamental challenges in using GPs is that the efficacy of a model is conferred by selecting an appropriate kernel and the associated hyperparameter values for a given problem. Furthermore, the training of GPs, that is optimizing the hyperparameters using a data set is traditionally performed using a cost function that is a weighted sum of data fit and model complexity, and the underlying trade-off is completely ignored. Addressing these challenges and shortcomings, in this article, we propose the following automated training scheme. Firstly, we use a weighted product of multiple kernels with a view to relieve the users from choosing an appropriate kernel for the problem at hand without any domain specific knowledge. Secondly, for the first time, we modify GP training by using a multi-objective optimizer to tune the hyperparameters and weights of multiple kernels and extract an approximation of the complete trade-off front between data-fit and model complexity. We then propose to use a novel solution selection strategy based on mean standardized log loss (MSLL) to select a solution from the estimated trade-off front and finalise training of a GP model. The results on three data sets and comparison with the standard approach clearly show the potential benefit of the proposed approach of using multi-objective optimization with multiple kernels.Natural Environment Research Council (NERC
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