997 research outputs found

    Measuring the energy intensity of domestic activities from smart meter data

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    Household electricity consumption can be broken down to appliance end-use through a variety of methods such as modelling, sub-metering, load disaggregation or non-intrusive appliance load monitoring (NILM). We advance and complement this important field of energy research through an innovative methodology that characterises the energy consumption of domestic life by making the linkages between appliance end-use and activities through an ontology built from qualitative data about the household and NILM data. We use activities as a descriptive term for the common ways households spend their time at home. These activities, such as cooking or laundering, are meaningful to households’ own lived experience. Thus, besides strictly technical algorithmic approaches for processing quantitative smart meter data, we also draw on social science time use approaches and interview and ethnography data. Our method disaggregates a households total electricity load down to appliance level and provides the start time, duration, and total electricity consumption for each occurrence of appliance usage. We then make inferences about activities occurring in the home by combining these disaggregated data with an ontology that formally specifies the relationships between electricity-using appliances and activities. We also propose two novel standardised metrics to enable easy quantifiable comparison within and across households of the energy intensity and routine of activities of interest. Finally, we demonstrate our results over a sample of ten households with an in-depth analysis of which activities can be inferred with the qualitative and quantitative data available for each household at any time, and the level of accuracy with which each activity can be inferred, unique to each household. This work has important applications from providing meaningful energy feedback to households to comparing the energy efficiency of households’ daily activities, and exploring the potential to shift the timing of activities for demand management

    The First Implementation of Respiratory Triggered 4DCBCT on a Linear Accelerator

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    Four Dimensional Cone Beam Computed Tomography (4DCBCT) is an image guidance strategy used for patient positioning in radiotherapy. In conventional implementations of 4DCBCT, a constant gantry speed and a constant projection pulse rate are used. Unfortunately, this leads to higher imaging doses than are necessary because a large number of redundant projections are acquired. In theoretical studies, we have previously demonstrated that by suppressing redundant projections the imaging dose can be reduced by 40-50% for a majority of patients with little reduction in image quality. The aim of this study was to experimentally realise the projection suppression technique, which we have called Respiratory Triggered 4DCBCT (RT-4DCBCT). A real-time control system was developed that takes the respiratory signal as input and computes whether to acquire, or suppress, the next projection trigger during 4DCBCT acquisition. The CIRS dynamic thorax phantom was programmed with a 2cm peak-to-peak motion and periods ranging from 2 to 8 seconds. Image quality was assessed by computing the edge response width of a 3cm imaging insert placed in the phantom as well as the signal to noise ratio of the phantoms tissue and the contrast to noise ratio between the phantoms lung and tissue. The standard deviation in the Superior-Inferior direction of the 3cm imaging insert was used to assess intra-phase bin displacement variations with a higher standard deviation implying more motion blur. The 4DCBCT imaging dose was reduced by 8.6%, 41%, 54%, 70% and 77% for patients with 2, 3, 4, 6 and 8 second breathing periods respectively when compared to conventional 4DCBCT. The standard deviation of the intra-phase bin displacement variation of the 3cm imaging insert was reduced by between 13% and 43% indicating a more consistent position for the projections within respiratory phases. For the 4 second breathing period, the edge response width was reduced by 39% (0.8mm) with only a 6-7% decrease in the signal to noise and contrast to noise ratios. RT-4DCBCT has been experimentally realised and reduced to practice on a linear accelerator with a measurable imaging dose reductions over conventional 4DCBCT and little degradation in image quality

    Autonomous Gait Event Detection with Portable Single-Camera Gait Kinematics Analysis System

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    Laboratory-based nonwearable motion analysis systems have significantly advanced with robust objective measurement of thelimb motion, resulting in quantified, standardized, and reliable outcome measures compared with traditional, semisubjective,observational gait analysis. However, the requirement for large laboratory space and operational expertise makes these systemsimpractical for gait analysis at local clinics and homes. In this paper, we focus on autonomous gait event detection with our bespoke,relatively inexpensive, and portable, single-camera gait kinematics analysis system. Our proposed systemincludes video acquisitionwith camera calibration, Kalman filter + Structural-Similarity-based marker tracking, autonomous knee angle calculation, videoframe-identification-based autonomous gait event detection, and result visualization. The only operational effort required is themarker-template selection for tracking initialization, aided by an easy-to-use graphic user interface.The knee angle validation on10 stroke patients and 5 healthy volunteers against a gold standard optical motion analysis system indicates very good agreement.The autonomous gait event detection shows high detection rates for all gait events. Experimental results demonstrate that theproposed system can automatically measure the knee angle and detect gait events with good accuracy and thus offer an alternative,cost-effective, and convenient solution for clinical gait kinematics analysis

    Component-Based Real-Time Operating System for Embedded Applications

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    Acceptance rate: 37%, Rank (CORE): AInternational audienceAs embedded systems must constantly integrate new functionalities, their developement cycles must be based on high-level abstractions, making the software design more flexible. CBSE provides an approach to these new requirements. However, low-level services provided by operating systems are an integral part of embedded applications, furthermore deployed on resource-limited devices. Therefore, the expected benefits of CBSE must not impact on the constraints imposed by the targetted domain, such as memory footprint, energy consumption, and execution time. In this paper, we present the componentization of a legacy industry-established Real-Time Operating System, and how component-based applications are built on top of it. We use the Think framework that allows to produce flexible systems while paying for flexibility only where desired. Performed experimentions show that the induced overhead is negligeable

    Transient deSUMOylation of IRF2BP proteins controls early transcription in EGFR signaling

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    Molecular switches are essential modules in signaling networksand transcriptional reprogramming. Here, we describe a role forsmall ubiquitin-related modifier SUMO as a molecular switch inepidermal growth factor receptor (EGFR) signaling. Using quantita-tive mass spectrometry, we compare the endogenous SUMOproteomes of HeLa cells before and after EGF stimulation. Thereby,we identify a small group of transcriptional coregulators includingIRF2BP1, IRF2BP2, and IRF2BPL as novel players in EGFR signaling.Comparison of cells expressing wild type or SUMOylation-deficientIRF2BP1indicates that transient deSUMOylation of IRF2BP proteinsis important for appropriate expression of immediate early genesincludingdual specificity phosphatase1(DUSP1, MKP-1) and thetranscription factor ATF3. We find that IRF2BP1is a repressor,whose transient deSUMOylation on the DUSP1promoter allows—and whose timely reSUMOylation restricts—DUSP1transcription.Our work thus provides a paradigm how comparative SUMOproteome analyses serve to reveal novel regulators in signal trans-duction and transcription

    CCL2 and CCR2 regulate pain-related behaviour and early gene expression in post-traumatic murine osteoarthritis but contribute little to chondropathy

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    SummaryObjectiveThe role of inflammation in structural and symptomatic osteoarthritis (OA) remains unclear. One key mediator of inflammation is the chemokine CCL2, primarily responsible for attracting monocytes to sites of injury. We investigated the role of CCL2 and its receptor CCR2 in experimental OA.DesignOA was induced in 10 weeks old male wild type (WT), Ccl2−/− and Ccr2−/− mice, by destabilisation of the medial meniscus (DMM). RNA was extracted from whole joints at 6 h and 7 days post-surgery and examined by reverse transcription polymerase chain reaction (RT-PCR). Gene expression changes between naïve and DMM-operated mice were compared. Chondropathy scores, from mice at 8, 12, 16 and 20 weeks post DMM were calculated using modified Osteoarthritis Research Society International (OARSI) grading systems. Changes in hind paw weight distribution, as a measure of pain, were assessed by Linton incapacitance.ResultsAbsence of CCL2 strongly suppressed (>90%) selective inflammatory response genes in the joint 6 h post DMM, including arginase 1, prostaglandin synthase 2, nitric oxide synthase 2 and inhibin A. IL6, MMP3 and tissue inhibitor of metalloproteinase 1 were also significantly suppressed. Similar trends were also observed in the absence of CCR2. A lower average chondropathy score was observed in both Ccl2−/− and Ccr2−/− mice at 12, 16 and 20 weeks post DMM compared with WT mice, but this was only statistically significant at 20 weeks in Ccr2−/− mice. Pain-related behaviour in Ccl2−/− and Ccr2−/− mice post DMM was delayed in onset.ConclusionThe CCL2/CCR2 axis plays an important role in the development of pain in murine OA, but contributes little to cartilage damage

    Telomere length predicts progression and overall survival in chronic lymphocytic leukemia: data from the UK LRF CLL4 trial

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    Telomere erosion and fusion play an important role in the pathology of many common human malignancies including CLL.1,2 Previous studies in CLL have shown that short telomeres defined on the basis of the median value or receiver operating characteristic (ROC) analysis are associated with unmutated IGHV genes, poor risk genomic abnormalities, genomic complexity and high expression of CD38, CD49d, and ZAP70 whereas long telomeres are associated with increasing IGHV mutational load, isolated deletion of 13q and low CD49d expression. In addition, in predominantly diagnostic or mixed patient cohorts, telomere length (TL) predicts time to first treatment and/or overall survival (OS) in multivariate analyses of models incorporating established biomarkers. 3-7 However uncertainties about the most clinically relevant measure of telomere length, the optimal choice of assay, the need for assay standardisation and the lack of published data on the prognostic value of TL in patients entered into randomised trials have hindered the implementation of TL measurement into routine clinical practice. We have attempted to address these issues by measuring telomere length using monochrome multiplex Q-PCR (MMQ-PCR) in 384 patients at randomisation into the UK LRF CLL4 phase 3 chemotherapy trial (Table S1), of whom 111 samples were also screened by single telomer
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