220 research outputs found

    Interdisciplinary Object-Oriented Domain Analysis for Electronic Medical Records

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    The experience gained during the domain analysis for data models of electronic medical records is discussed. Topics of interest are the way in which the domain is analyzed by means of expert interviews, the observed need for parallelism in the learning process, object-oriented modeling of the results, tool support for rapid evaluation of models with an object-oriented database, and an assessment of the requirements on electronic medical records. The emphasis of this paper is to discuss the process of participatory analysis of the domain for electronic medical records in an interdisciplinary setting. Some extracts of the results of the domain analysis are presented

    E-Commerce in der Entsorgungsindustrie: Eine E-Commerce-Lösung fĂŒr Dienstleistungen als Instrument zur Kundenbindung in der Entsorgungsindustrie

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    Dynamische MĂ€rkte mit rasch wandelnden KundenbedĂŒrfnissen, neuen unerwarteten globalen Konkurrenten und raschem technologischen Wandel sind die Effekte der ,informationstechnischen Revolution’ der letzten zwei Jahrzehnte

    ALLocator: An Interactive Web Platform for the Analysis of Metabolomic LC-ESI-MS Datasets, Enabling Semi-Automated, User-Revised Compound Annotation and Mass Isotopomer Ratio Analysis

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    Kessler N, Walter F, Persicke M, et al. ALLocator: An Interactive Web Platform for the Analysis of Metabolomic LC-ESI-MS Datasets, Enabling Semi-Automated, User-Revised Compound Annotation and Mass Isotopomer Ratio Analysis. PLoS ONE. 2014;9(11): e113909.Adduct formation, fragmentation events and matrix effects impose special challenges to the identification and quantitation of metabolites in LC-ESI-MS datasets. An important step in compound identification is the deconvolution of mass signals. During this processing step, peaks representing adducts, fragments, and isotopologues of the same analyte are allocated to a distinct group, in order to separate peaks from coeluting compounds. From these peak groups, neutral masses and pseudo spectra are derived and used for metabolite identification via mass decomposition and database matching. Quantitation of metabolites is hampered by matrix effects and nonlinear responses in LC-ESI-MS measurements. A common approach to correct for these effects is the addition of a U-13C-labeled internal standard and the calculation of mass isotopomer ratios for each metabolite. Here we present a new web-platform for the analysis of LC-ESI-MS experiments. ALLocator covers the workflow from raw data processing to metabolite identification and mass isotopomer ratio analysis. The integrated processing pipeline for spectra deconvolution “ALLocatorSD” generates pseudo spectra and automatically identifies peaks emerging from the U-13C-labeled internal standard. Information from the latter improves mass decomposition and annotation of neutral losses. ALLocator provides an interactive and dynamic interface to explore and enhance the results in depth. Pseudo spectra of identified metabolites can be stored in user- and method-specific reference lists that can be applied on succeeding datasets. The potential of the software is exemplified in an experiment, in which abundance fold-changes of metabolites of the l-arginine biosynthesis in C. glutamicum type strain ATCC 13032 and l-arginine producing strain ATCC 21831 are compared. Furthermore, the capability for detection and annotation of uncommon large neutral losses is shown by the identification of (γ-)glutamyl dipeptides in the same strains. ALLocator is available online at: https://allocator.cebitec.uni-bielefeld.​de. A login is required, but freely available

    Lsd1 ablation triggers metabolic reprogramming of brown adipose tissue

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    Previous work indicated that lysine-specific demethylase 1 (Lsd1) can positively regulate the oxidative and thermogenic capacities of white and beige adipocytes. Here we investigate the role of Lsd1 in brown adipose tissue (BAT) and find that BAT- selective Lsd1 ablation induces a shift from oxidative to glycolytic metabolism. This shift is associated with downregulation of BAT-specific and upregulation of white adipose tissue (WAT)-selective gene expression. This results in the accumulation of di- and triacylglycerides and culminates in a profound whitening of BAT in aged Lsd1- deficient mice. Further studies show that Lsd1 maintains BAT properties via a dual role. It activates BAT-selective gene expression in concert with the transcription factor Nrf1 and represses WAT-selective genes through recruitment of the CoREST complex. In conclusion, our data uncover Lsd1 as a key regulator of gene expression and metabolic function in BAT

    Unmet needs in the diagnosis and treatment of dyslipidemia in the primary care setting in Germany

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    Objectives and methods: DETECT is a cross-sectional study of 55,518 unselected consecutive patients in 3188 representative primary care offices in Germany. In a random subset of 7519 patients, an extensive standardized laboratory program was undertaken. The study investigated the prevalence of cardiovascular disease, known risk factors (such as diabetes, hypertension and dyslipidemia and their co-morbid manifestation), as well as treatment patterns. The present analysis of the DETECT laboratory dataset focused on the prevalence and treatment of dyslipidemia in primary medical care in Germany. Coronary artery disease (CAD), risk categories and LDL-C target achievement rates were determined in the subset of 6815 patients according to the National Cholesterol Education Program (NCEP) ATP III Guidelines. Results: Of all patients, 54.3% had dyslipidemia. Only 54.4% of the NCEP-classified dyslipidemic patients were diagnosed as ‘dyslipidemic’ by their physicians. Only 27% of all dyslipidemic patients (and 40.7% of the recognized dyslipidemic patients) were treated with lipid-lowering medications, and 11.1% of all dyslipidemic patients (41.4% of the patients treated with lipid-lowering drugs) achieved their LDL-C treatment goals. In conclusion, 80.3% of patients in the sample with dyslipidemia went undiagnosed, un-treated or under-treated

    Rahmenkonzept der Hochschulen des Landes Baden-WĂŒrttemberg fĂŒr datenintensive Dienste – bwDATA Phase III (2020-2024)

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    Das zentrale Ziel von bwDATA in Phase III ist die optimale UnterstĂŒtzung der Wissenschaft in den Belangen der Datenspeicherung und des nachhaltigen Forschungsdatenmanagements ebenso wie die Versorgung der Landeshochschulen mit auf ihre jeweiligen Belange und BedĂŒrfnisse angepassten Speicherstrukturen und darauf basierenden Diensten. Dem Beispiel des bwHPC-Konzepts folgend werden hierbei enge Abstimmung, Kooperation und Arbeitsteilung zwischen den beteiligten Einrichtungen vertieft. Das vorliegende Rahmenkonzept soll dabei nicht als absoluter Leitfaden fĂŒr die Periode 2020 bis 2024 dienen, es will vielmehr fĂŒr die verschiedenen Bereiche der Wissenschaft, fĂŒr Forschung, Lehre und Administration die Rahmenbedingungen fĂŒr den koordinierten Aufbau und Betrieb speicherintensiver Dienste definieren. bwDATA basiert dabei auf einer gemeinsamen, strategischen Vorgehensweise aller UniversitĂ€ten, Hochschulen der angewandten Wissenschaften, PĂ€dagogischen Hochschulen, Kunst- und Musikhochschulen, der Dualen Hochschule Baden-WĂŒrttembergs, der Landesbibliotheken und des Landesarchivs. Ein wesentliches Ziel von bwDATA Phase III ist der verbesserte Umgang mit großen wissenschaftlichen Datenmengen ĂŒber den gesamten Data Life Cycle in der BaWĂŒ-Datenföderation und damit auch der verstĂ€rkte Aufbau des Forschungsdatenmanagements fĂŒr die beteiligten wissenschaftlichen Einrichtungen bis hin zu Backup und Langzeitarchivierung. Das Rahmenkonzept bwDATA definiert die Möglichkeit, die Wissenschaft in den Teilgebieten Forschung, Lehre und Administration durch Verbessern vorhandener und Aufbau neuer Lösungen flexibel zu unterstĂŒtzen

    Probing the SELEX Process with Next-Generation Sequencing

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    Background SELEX is an iterative process in which highly diverse synthetic nucleic acid libraries are selected over many rounds to finally identify aptamers with desired properties. However, little is understood as how binders are enriched during the selection course. Next-generation sequencing offers the opportunity to open the black box and observe a large part of the population dynamics during the selection process. Methodology We have performed a semi-automated SELEX procedure on the model target streptavidin starting with a synthetic DNA oligonucleotide library and compared results obtained by the conventional analysis via cloning and Sanger sequencing with next-generation sequencing. In order to follow the population dynamics during the selection, pools from all selection rounds were barcoded and sequenced in parallel. Conclusions High affinity aptamers can be readily identified simply by copy number enrichment in the first selection rounds. Based on our results, we suggest a new selection scheme that avoids a high number of iterative selection rounds while reducing time, PCR bias, and artifacts

    Citizen science’s transformative impact on science, citizen empowerment and socio-political processes

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    Citizen science (CS) can foster transformative impact for science, citizen empowerment and socio-political processes. To unleash this impact, a clearer understanding of its current status and challenges for its development is needed. Using quantitative indicators developed in a collaborative stakeholder process, our study provides a comprehensive overview of the current status of CS in Germany, Austria and Switzerland. Our online survey with 340 responses focused on CS impact through (1) scientific practices, (2) participant learning and empowerment, and (3) socio-political processes. With regard to scientific impact, we found that data quality control is an established component of CS practice, while publication of CS data and results has not yet been achieved by all project coordinators (55%). Key benefits for citizen scientists were the experience of collective impact (“making a difference together with others”) as well as gaining new knowledge. For the citizen scientists’ learning outcomes, different forms of social learning, such as systematic feedback or personal mentoring, were essential. While the majority of respondents attributed an important value to CS for decision-making, only few were confident that CS data were indeed utilized as evidence by decision-makers. Based on these results, we recommend (1) that project coordinators and researchers strengthen scientific impact by fostering data management and publications, (2) that project coordinators and citizen scientists enhance participant impact by promoting social learning opportunities and (3) that project initiators and CS networks foster socio-political impact through early engagement with decision-makers and alignment with ongoing policy processes. In this way, CS can evolve its transformative impact
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