101 research outputs found

    CreaTology: Patterns in Digital Creative Arts

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    This special session presents research work on patterns in interdisciplinary areas, such as social network analyses, creative deception, and musicology with stringology. The work presented here is encouraging and opens up opportunities for potential further research and development

    Predicting Alzheimers Disease Diagnosis Risk over Time with Survival Machine Learning on the ADNI Cohort

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    The rise of Alzheimers Disease worldwide has prompted a search for efficient tools which can be used to predict deterioration in cognitive decline leading to dementia. In this paper, we explore the potential of survival machine learning as such a tool for building models capable of predicting not only deterioration but also the likely time to deterioration. We demonstrate good predictive ability (0.86 C-Index), lending support to its use in clinical investigation and prediction of Alzheimers Disease risk

    A Machine Learning Approach for Predicting Deterioration in Alzheimer's Disease

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    This paper explores deterioration in Alzheimer’s Disease using Machine Learning. Subjects were split into two datasets based on baseline diagnosis (Cognitively Normal, Mild Cognitive Impairment), with outcome of deterioration at final visit (a binomial essentially yes/no categorisation) using data from the Alzheimer’s Disease Neuroimaging Initiative (demographics, genetics, CSF, imaging, and neuropsychological testing etc). Six machine learning models, including gradient boosting, were built, and evaluated on these datasets using a nested cross-validation procedure, with the best performing models being put through repeated nested cross-validation at 100 iterations. We were able to demonstrate good predictive ability using CART predicting which of those in the cognitively normal group deteriorated and received a worse diagnosis (AUC = 0.88). For the mild cognitive impairment group, we were able to achieve good predictive ability for deterioration with Elastic Net (AUC = 0.76)

    Improving time-efficiency in blocking expanding ring search for mobile ad hoc networks

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    We propose a new strategy for reducing the amount of latency and energy consumption in Blocking Expanding Ring Search (BERS) and enhanced Blocking Expanding Ring Search (BERS*) for mobile ad hoc networks (MANETs). BERS and BERS* are respectively energy and energy–time efficient route discovery protocols for MANETs as compared to conventional Expanding Ring Search (ERS). In this study, we identify unnecessary waiting time caused by a STOP/END instruction in BERS/BERS* and explore the potential of further improvement of their time efficiency. This leads to tBERS and tBERS*, the improved BERS and BERS* respectively. In tBERS/tBERS*, a route node may also issue the STOP/END instruction to terminate flooding. We implement this idea in algorithms, conduct analysis, and achieve further latency reduction in both tBERS and tBERS* as well as the energy saving in tBERS*

    N-body simulations of planet formation via pebble accretion I:First Results

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    Context. Planet formation with pebbles has been proposed to solve a couple of long-standing issues in the classical formation model. Some sophisticated simulations have been done to confirm the efficiency of pebble accretion. However, there has not been any global N-body simulations that compare the outcomes of planet formation via pebble accretion with observed extrasolar planetary systems. Aims. In this paper, we study the effects of a range of initial parameters of planet formation via pebble accretion, and present the first results of our simulations. Methods. We incorporate the pebble accretion model by Ida et al. (2016) in the N-body code SyMBA (Duncan et al. 1998), along with the effects of gas accretion, eccentricity and inclination damping and planet migration in the disc. Results. We confirm that pebble accretion leads to a variety of planetary systems, but have difficulty in reproducing observed properties of exoplanetary systems, such as planetary mass, semimajor axis, and eccentricity distributions. The main reason behind this is a too-efficient type I migration, which sensitively depends on the disc model. However, our simulations also lead to a few interesting predictions. First, we find that formation efficiencies of planets depend on the stellar metallicities, not only for giant planets, but also for Earths (Es) and Super-Earths (SEs). The dependency for Es/SEs is subtle. Although higher metallicity environments lead to faster formation of a larger number of Es/SEs, they also tend to be lost later via dynamical instability. Second, our results indicate that a wide range of bulk densities observed for Es and SEs is a natural consequence of dynamical evolution of planetary systems. Third, the ejection trend of our simulations suggest that one free-floating E/SE may be expected for two smaller-mass planets.Comment: Accepted for publication in A&A, 21 pages, 15 figure

    Finishing the euchromatic sequence of the human genome

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    The sequence of the human genome encodes the genetic instructions for human physiology, as well as rich information about human evolution. In 2001, the International Human Genome Sequencing Consortium reported a draft sequence of the euchromatic portion of the human genome. Since then, the international collaboration has worked to convert this draft into a genome sequence with high accuracy and nearly complete coverage. Here, we report the result of this finishing process. The current genome sequence (Build 35) contains 2.85 billion nucleotides interrupted by only 341 gaps. It covers ∼99% of the euchromatic genome and is accurate to an error rate of ∼1 event per 100,000 bases. Many of the remaining euchromatic gaps are associated with segmental duplications and will require focused work with new methods. The near-complete sequence, the first for a vertebrate, greatly improves the precision of biological analyses of the human genome including studies of gene number, birth and death. Notably, the human enome seems to encode only 20,000-25,000 protein-coding genes. The genome sequence reported here should serve as a firm foundation for biomedical research in the decades ahead

    Charge Transport in Two-Photon Semiconducting Structures for Solar Fuels

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