6,860 research outputs found

    Discovering common hidden causes in sequences of events

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    FLAGS : a methodology for adaptive anomaly detection and root cause analysis on sensor data streams by fusing expert knowledge with machine learning

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    Anomalies and faults can be detected, and their causes verified, using both data-driven and knowledge-driven techniques. Data-driven techniques can adapt their internal functioning based on the raw input data but fail to explain the manifestation of any detection. Knowledge-driven techniques inherently deliver the cause of the faults that were detected but require too much human effort to set up. In this paper, we introduce FLAGS, the Fused-AI interpretabLe Anomaly Generation System, and combine both techniques in one methodology to overcome their limitations and optimize them based on limited user feedback. Semantic knowledge is incorporated in a machine learning technique to enhance expressivity. At the same time, feedback about the faults and anomalies that occurred is provided as input to increase adaptiveness using semantic rule mining methods. This new methodology is evaluated on a predictive maintenance case for trains. We show that our method reduces their downtime and provides more insight into frequently occurring problems. (C) 2020 The Authors. Published by Elsevier B.V

    Reciprocal Sign Epistasis between Frequently Experimentally Evolved Adaptive Mutations Causes a Rugged Fitness Landscape

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    The fitness landscape captures the relationship between genotype and evolutionary fitness and is a pervasive metaphor used to describe the possible evolutionary trajectories of adaptation. However, little is known about the actual shape of fitness landscapes, including whether valleys of low fitness create local fitness optima, acting as barriers to adaptive change. Here we provide evidence of a rugged molecular fitness landscape arising during an evolution experiment in an asexual population of Saccharomyces cerevisiae. We identify the mutations that arose during the evolution using whole-genome sequencing and use competitive fitness assays to describe the mutations individually responsible for adaptation. In addition, we find that a fitness valley between two adaptive mutations in the genes MTH1 and HXT6/HXT7 is caused by reciprocal sign epistasis, where the fitness cost of the double mutant prohibits the two mutations from being selected in the same genetic background. The constraint enforced by reciprocal sign epistasis causes the mutations to remain mutually exclusive during the experiment, even though adaptive mutations in these two genes occur several times in independent lineages during the experiment. Our results show that epistasis plays a key role during adaptation and that inter-genic interactions can act as barriers between adaptive solutions. These results also provide a new interpretation on the classic Dobzhansky-Muller model of reproductive isolation and display some surprising parallels with mutations in genes often associated with tumors

    Dynamic Maps: Representations of Change in Geospatial Modeling and Visualization

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    By coining the descriptive phrase ―user-centric geographic cosmology, Goodchild (1998), challenges the geographically oriented to address GIS in the broadest imaginable context: as interlocutor between persons and geo-phenomena. This investigation responds both in a general way, and more specifically, to the representations of change in GIS modeling and visualization leading to dynamic mapping. The investigation, consisting of a report and a series of experiments, explores and demonstrates prototype workarounds that enhance GIS capabilities by drawing upon ideas, techniques, and components from agent-based modeling and visualization software, and suggests shifts at the conceptual, methodological, and technical levels. The workarounds and demonstrations presented here are four-dimensional visualizations, representing changes and behaviors of different types of entities such as living creatures, mobile assets, features, structures, and surfaces, using GIS, agent-based modeling and animation techniques. In a typical case, a creature begins as a point feature in GIS, becomes a mobile and interactive object in agent-based modeling, and is fleshed out to three dimensions in an animated representation. In contrast, a land surface remains much the same in all three stages. The experiments address change in location, orientation, shape, visual attributes, viewpoint, scale, and speed in applications representing predator-prey, search and destroy, sense and locate and urban sprawl. During the experiments, particular attention is paid to factors of modeling and visualization involved in engaging human sensing and cognitive abilities

    COMPARATIVE MAPPING: HOMOLOGY WITHIN THE ORDER PERISSODACTYLA OF FOUR GENES LOCATED ON EQUUS CABALLUS CHROMOSOME 20

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    Since changes in chromosome morphology contribute to the knowledge of evolution as well as to chromosome dynamics, this study looks specifically at one chromosome compared in twelve different species of Perissodactyls: Equus caballus (ECA), E. przewalskii (EPR), Equus africanus somaliensis (EAF), E. asinus (EAS), E. hemionus onager (EHO), E. h. kulan (EHK), E. h. kiang (EKI), E. zebra hartmannae (EZH), E. grevyi (EGR), E. burchelli (EBU), Tapirus indicus (TIN), and Rhinoceros unicornis (RUN). While chromosome morphology studies have been done in some of the extant equids, none have followed the evolution of this chromosome, homologous to Equus caballus chromosome 20 (ECA20), which contains the major histocompatibility complex (MHC). The gene order on the chromosome arm homologous to human chromosome six in most Equidae is reversed with respect to the centromere in comparison to humans. Multicolor fluorescence in situ hybridization was used to show that four probes from ECA20 hybridized to ECA20 (control), SWA5, EAS8, EHO16, EHK14, EKI16, EZH10, EGR11, EBU13, TIN4, and one of RUN12, 14, 15, or 22. The order for the four genes in the horses, zebras, and rhinoceros were as follows: cen-EDN1-MHC-ITPR3-MUT. Hybridization to the ass and tapir chromosomes displayed a possible neocentromere formation. It is apparent the chromosome has gone through several morphological changes while undergoing speciation in the Equidae, yet the overall gene order is conserved

    The Pinhole/Occulter Facility

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    Scientific objectives and requirements are discussed for solar X-ray observations, coronagraph observations, studies of coronal particle acceleration, and cosmic X-ray observations. Improved sensitivity and resolution can be provided for these studies using the pinhole/occulter facility which consists of a self-deployed boom of 50 m length separating an occulter plane from a detector plane. The X-ray detectors and coronagraphic optics mounted on the detector plane are analogous to the focal plane instrumentation of an ordinary telescope except that they use the occulter only for providing a shadow pattern. The occulter plane is passive and has no electrical interface with the rest of the facility

    Novel variation and <i>de novo </i>mutation rates in population-wide <i>de novo</i> assembled Danish trios

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    Building a population-specific catalogue of single nucleotide variants (SNVs), indels and structural variants (SVs) with frequencies, termed a national pan-genome, is critical for further advancing clinical and public health genetics in large cohorts. Here we report a Danish pan-genome obtained from sequencing 10 trios to high depth (50 × ). We report 536k novel SNVs and 283k novel short indels from mapping approaches and develop a population-wide de novo assembly approach to identify 132k novel indels larger than 10 nucleotides with low false discovery rates. We identify a higher proportion of indels and SVs than previous efforts showing the merits of high coverage and de novo assembly approaches. In addition, we use trio information to identify de novo mutations and use a probabilistic method to provide direct estimates of 1.27e−8 and 1.5e−9 per nucleotide per generation for SNVs and indels, respectively
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