9 research outputs found

    Structure learning and optimisation in a Markov-network based estimation of distribution algorithm

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    Structure learning is a crucial component of a multivariate Estimation of Distribution algorithm. It is the part which determines the interactions between variables in the probabilistic model, based on analysis of the fitness function or a population. In this paper we take three different approaches to structure learning in an EDA based on Markov networks and use measures from the information retrieval community (precision, recall and the F-measure) to assess the quality of the structures learned. We then observe the impact that structure has on the fitness modelling and optimisation capabilities of the resulting model, concluding that these results should be relevantto research in both structure learning and fitness modeling. © 2009 IEEE

    Approaches to selection and their effect on fitness modelling in an Estimation of Distribution Algorithm

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    Selection is one of the defining characteristics of an evolutionary algorithm, yet inherent in the selection process is the loss of some information from a population. Poor solutions may provide information about how to bias the search toward good solutions. Many Estimation of Distribution Algorithms (EDAs) use truncation selection which discards all solutions below a certain fitness, thus losing this information. Our previous work on Distribution Estimation using Markov networks (DEUM) has described an EDA which constructs a model of the fitness function; a unique feature of this approach is that because selective pressure is built into the model itself selection becomes optional. This paper outlines a series of experiments which make use of this property to examine the effects of selection on the population. We look at the impact of selecting only highly fit solutions, only poor solutions, selecting a mixture of highly fit and poor solutions, and abandoning selection altogether. We show that in some circumstances, particularly where some information about the problem is already known, selection of the fittest only is suboptimal. © 2008 IEEE

    A systematic approach to parameter optimization and its application to flight schedule simulation software

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    Industrial software often has many parameters that critically impact performance. Frequently, these are left in a sub-optimal configuration for a given application because searching over possible configurations is costly and, except for developer instinct, the relationships between parameters and performance are often unclear and complex. While there have been significant advances in automated parameter tuning approaches recently, they are typically black-box. The high-quality solutions produced are returned to the user without explanation. The nature of optimisation means that, often, these solutions are far outside the well-established settings for the software, making it difficult to accept and use them. To address the above issue, a systematic approach to software parameter optimization is presented. Several well-established techniques are followed in sequence, each underpinning the next, with rigorous analysis of the search space. This allows the results to be explainable to both end users and developers, improving confidence in the optimal solutions, particularly where they are counter-intuitive. The process comprises statistical analysis of the parameters; single-objective optimization for each target objective; functional ANOVA to explain trends and inter-parameter interactions; and a multi-objective optimization seeded with the results from the single-objective stage. A case study demonstrates application to business-critical software developed by the international airline Air France-KLM for measuring flight schedule robustness. A configuration is found with a run-time of 80% that of the tried-and-tested configuration, with no loss in predictive accuracy. The configuration is supplemented with detailed analysis explaining the importance of each parameter, how they interact with each other, how they influence run-time and accuracy, and how the final configuration was reached. In particular, this explains why the configuration included some parameter settings that were outwith the usually recommended range, greatly increasing developer confidence and encouraging adoption of the new configuration

    Thigh-length compression stockings and DVT after stroke

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    Controversy exists as to whether neoadjuvant chemotherapy improves survival in patients with invasive bladder cancer, despite randomised controlled trials of more than 3000 patients. We undertook a systematic review and meta-analysis to assess the effect of such treatment on survival in patients with this disease

    Azithromycin in patients admitted to hospital with COVID-19 (RECOVERY): a randomised, controlled, open-label, platform trial

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    Background Azithromycin has been proposed as a treatment for COVID-19 on the basis of its immunomodulatory actions. We aimed to evaluate the safety and efficacy of azithromycin in patients admitted to hospital with COVID-19. Methods In this randomised, controlled, open-label, adaptive platform trial (Randomised Evaluation of COVID-19 Therapy [RECOVERY]), several possible treatments were compared with usual care in patients admitted to hospital with COVID-19 in the UK. The trial is underway at 176 hospitals in the UK. Eligible and consenting patients were randomly allocated to either usual standard of care alone or usual standard of care plus azithromycin 500 mg once per day by mouth or intravenously for 10 days or until discharge (or allocation to one of the other RECOVERY treatment groups). Patients were assigned via web-based simple (unstratified) randomisation with allocation concealment and were twice as likely to be randomly assigned to usual care than to any of the active treatment groups. Participants and local study staff were not masked to the allocated treatment, but all others involved in the trial were masked to the outcome data during the trial. The primary outcome was 28-day all-cause mortality, assessed in the intention-to-treat population. The trial is registered with ISRCTN, 50189673, and ClinicalTrials.gov, NCT04381936. Findings Between April 7 and Nov 27, 2020, of 16 442 patients enrolled in the RECOVERY trial, 9433 (57%) were eligible and 7763 were included in the assessment of azithromycin. The mean age of these study participants was 65·3 years (SD 15·7) and approximately a third were women (2944 [38%] of 7763). 2582 patients were randomly allocated to receive azithromycin and 5181 patients were randomly allocated to usual care alone. Overall, 561 (22%) patients allocated to azithromycin and 1162 (22%) patients allocated to usual care died within 28 days (rate ratio 0·97, 95% CI 0·87–1·07; p=0·50). No significant difference was seen in duration of hospital stay (median 10 days [IQR 5 to >28] vs 11 days [5 to >28]) or the proportion of patients discharged from hospital alive within 28 days (rate ratio 1·04, 95% CI 0·98–1·10; p=0·19). Among those not on invasive mechanical ventilation at baseline, no significant difference was seen in the proportion meeting the composite endpoint of invasive mechanical ventilation or death (risk ratio 0·95, 95% CI 0·87–1·03; p=0·24). Interpretation In patients admitted to hospital with COVID-19, azithromycin did not improve survival or other prespecified clinical outcomes. Azithromycin use in patients admitted to hospital with COVID-19 should be restricted to patients in whom there is a clear antimicrobial indication. Funding UK Research and Innovation (Medical Research Council) and National Institute of Health Research
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