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Now showing 1 - 5 of 5
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    A new scenario framework for climate change research: The concept of shared socioeconomic pathways
    (Dordrecht [u.a.] : Springer, 2014) O'Neill, B.C.; Kriegler, E.; Riahi, K.; Ebi, K.L.; Hallegatte, S.; Carter, T.R.; Mathur, R.; van Vuuren, D.P.
    The new scenario framework for climate change research envisions combining pathways of future radiative forcing and their associated climate changes with alternative pathways of socioeconomic development in order to carry out research on climate change impacts, adaptation, and mitigation. Here we propose a conceptual framework for how to define and develop a set of Shared Socioeconomic Pathways (SSPs) for use within the scenario framework. We define SSPs as reference pathways describing plausible alternative trends in the evolution of society and ecosystems over a century timescale, in the absence of climate change or climate policies. We introduce the concept of a space of challenges to adaptation and to mitigation that should be spanned by the SSPs, and discuss how particular trends in social, economic, and environmental development could be combined to produce such outcomes. A comparison to the narratives from the scenarios developed in the Special Report on Emissions Scenarios (SRES) illustrates how a starting point for developing SSPs can be defined. We suggest initial development of a set of basic SSPs that could then be extended to meet more specific purposes, and envision a process of application of basic and extended SSPs that would be iterative and potentially lead to modification of the original SSPs themselves.
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    Testing versus proving in climate impact research
    (Wadern : Schloss Dagstuhl, 2013) Ionescu, C.; Jansson, P.
    Higher-order properties arise naturally in some areas of climate impact research. For example, "vulnerability measures", crucial in assessing the vulnerability to climate change of various regions and entities, must fulfill certain conditions which are best expressed by quantification over all increasing functions of an appropriate type. This kind of property is notoriously difficult to test. However, for the measures used in practice, it is quite easy to encode the property as a dependent type and prove it correct. Moreover, in scientific programming, one is often interested in correctness "up to implication": The program would work as expected, say, if one would use real numbers instead of floating-point values. Such counterfactuals are impossible to test, but again, they can be easily encoded as types and proven. We show examples of such situations (encoded in Agda), encountered in actual vulnerability assessments.
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    The genomic data deficit : On the need to inform research subjects of the informational content of their genomic sequence data in consent for genomic research
    (Amsterdam [u.a.] : Elsevier Science, 2020) Hallinan, Dara
    Research subject consent plays a significant role in the legitimation of genomic research in Europe – both ethically and legally. One key criterion for any consent to be legitimate is that the research subject is ‘informed’. This criterion implies that the research subject is given all relevant information to allow them to decide whether engaging with a genomic research infrastructure or project would be normatively desirable and whether they wish to accept the risks associated with engagement. This article makes the normative argument that, in order to be truly ‘informed’, the research subject should be provided with information on the informational content of their genomic sequence data. Information should be provided, in the first instance, prior to the initial consent transaction, and should include: information on the fact that genomic sequence data will be collected and processed, information on the types of information which can currently be extracted from sequence data and information on the uncertainties surrounding the types of information which may eventually be extractable from sequence data. Information should also be provided, on an ongoing basis, as relevant and necessary, throughout the research process, and should include: information on novel information which can be extracted from sequence data and information on the novel uses and utility of sequence data. The article argues that current elaborations of ‘informed’ consent fail to adequately address the requirements set out in the normative argument and that this inadequacy constitutes an issue in need of a solution. The article finishes with a set of observations as to the fora best suited to deliver a solution and as to the substantive content of a solution. © 2020 The Authors
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    Bridging the Gap Between (AI-) Services and Their Application in Research and Clinical Settings Through Interoperability: the OMI-Protocol
    (Hannover : Technische Informationsbibliothek, 2024-02) Sigle, Stefan; Werner, Patrick; Schweizer, Simon; Caldeira, Liliana; Hosch, René; Dyrba, Martin; Fegeler, Christian; Sigle, Stefan; Werner, Patrick; Schweizer, Simon; Caldeira, Liliana; Hosch, René; Dyrba, Martin; Fegeler, Christian; Grönke, Ana; Seletkov, Dmitrii; Kotter, Elmar; Nensa, Felix; Wehrle, Julius; Kaufmes, Kevin; Scherer, Lucas; Nolden, Marco; Boeker, Martin; Schmidt, Marvin; Pelka, Obioma; Braren, Rickmer; Stump, Shura-Roman; Graetz, Teresa; Pogarell, Tobias; Susetzky, Tobias; Wieland, Tobias; Parmar, Vicky; Wang, Yuanbin
    Artificial Intelligence (AI) in research and clinical contexts is transforming the areas of medical and life sciences permanently. Aspects like findability, accessibility, interoperability, and reusability are often neglected for AI-based inference services. The Open Medical Inference (OMI) protocol aims to support remote inference by addressing the aforementioned aspects. Key component of the proposed protocol is an interoperable registry for remote inference services, which addresses the issue of findability for algorithms. It is complemented by information on how to invoke services remotely. Together, these components lay the basis for the implementation of distributed inference services beyond organizational borders. The OMI protocol considers prior work for aspects like data representation and transmission standards wherever possible. Based on Business Process Modeling of prototypical use cases for the service registry and common inference processes, a generic information model for remote services was inferred. Based on this model, FHIR resources were identified to represent AI-based services. The OMI protocol is first introduced using AI-services in radiology but is designed to be generalizable to other application domains as well. It provides an accessible, open specification as blueprint for the introduction and implementation of remote inference services.
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    PID Network Deutschland: Netzwerk für die Förderung von persistenten Identifikatoren in Wissenschaft und Kultur
    (Potsdam : Helmholtz Open Science Office, 2023) Bertelmann, Roland; Buys, Matthew; Kett, Jürgen; Pampel, Heinz; Pieper, Dirk; Scholze, Frank; Sens, Irina; Burger, Felix; Dreyer, Britta; Glagla-Dietz, Stephanie; Hagemann- Wilholt, Stephanie; Hartmann, Sarah; Schrader, Antonia C.; Schirrwagen, Jochen; Summann, Friedrich; Vierkant, Paul
    [No abstract available]