96,078 research outputs found
A systematic literature review of cloud computing in eHealth
Cloud computing in eHealth is an emerging area for only few years. There
needs to identify the state of the art and pinpoint challenges and possible
directions for researchers and applications developers. Based on this need, we
have conducted a systematic review of cloud computing in eHealth. We searched
ACM Digital Library, IEEE Xplore, Inspec, ISI Web of Science and Springer as
well as relevant open-access journals for relevant articles. A total of 237
studies were first searched, of which 44 papers met the Include Criteria. The
studies identified three types of studied areas about cloud computing in
eHealth, namely (1) cloud-based eHealth framework design (n=13); (2)
applications of cloud computing (n=17); and (3) security or privacy control
mechanisms of healthcare data in the cloud (n=14). Most of the studies in the
review were about designs and concept-proof. Only very few studies have
evaluated their research in the real world, which may indicate that the
application of cloud computing in eHealth is still very immature. However, our
presented review could pinpoint that a hybrid cloud platform with mixed access
control and security protection mechanisms will be a main research area for
developing citizen centred home-based healthcare applications
The European Institute for Innovation through Health Data
The European Institute for Innovation through Health Data (i~HD, www.i-hd.eu) has been formed as one of the key sustainable entities arising from the Electronic Health Records for Clinical Research (IMI-JU-115189) and SemanticHealthNet (FP7-288408) projects, in collaboration with several other European projects and initiatives supported by the European Commission. i~HD is a European not-for-profit body, registered in Belgium through Royal Assent. i~HD has been established to tackle areas of challenge in the successful scaling up of innovations that critically rely on high-quality and interoperable health data. It will specifically address obstacles and opportunities to using health data by collating, developing, and promoting best practices in information governance and in semantic interoperability. It will help to sustain and propagate the results of health information and communication technology (ICT) research that enables better use of health data, assessing and optimizing their novel value wherever possible. i~HD has been formed after wide consultation and engagement of many stakeholders to develop methods, solutions, and services that can help to maximize the value obtained by all stakeholders from health data. It will support innovations in health maintenance, health care delivery, and knowledge discovery while ensuring compliance with all legal prerequisites, especially regarding the insurance of patient's privacy protection. It is bringing multiple stakeholder groups together so as to ensure that future solutions serve their collective needs and can be readily adopted affordably and at scale
Dwarna : a blockchain solution for dynamic consent in biobanking
Dynamic consent aims to empower research partners and facilitate active participation in the research process. Used within
the context of biobanking, it gives individuals access to information and control to determine how and where their
biospecimens and data should be used. We present Dwarna—a web portal for ‘dynamic consent’ that acts as a hub
connecting the different stakeholders of the Malta Biobank: biobank managers, researchers, research partners, and the
general public. The portal stores research partners’ consent in a blockchain to create an immutable audit trail of research
partners’ consent changes. Dwarna’s structure also presents a solution to the European Union’s General Data Protection
Regulation’s right to erasure—a right that is seemingly incompatible with the blockchain model. Dwarna’s transparent
structure increases trustworthiness in the biobanking process by giving research partners more control over which research
studies they participate in, by facilitating the withdrawal of consent and by making it possible to request that the biospecimen
and associated data are destroyed.peer-reviewe
Privacy in the Genomic Era
Genome sequencing technology has advanced at a rapid pace and it is now
possible to generate highly-detailed genotypes inexpensively. The collection
and analysis of such data has the potential to support various applications,
including personalized medical services. While the benefits of the genomics
revolution are trumpeted by the biomedical community, the increased
availability of such data has major implications for personal privacy; notably
because the genome has certain essential features, which include (but are not
limited to) (i) an association with traits and certain diseases, (ii)
identification capability (e.g., forensics), and (iii) revelation of family
relationships. Moreover, direct-to-consumer DNA testing increases the
likelihood that genome data will be made available in less regulated
environments, such as the Internet and for-profit companies. The problem of
genome data privacy thus resides at the crossroads of computer science,
medicine, and public policy. While the computer scientists have addressed data
privacy for various data types, there has been less attention dedicated to
genomic data. Thus, the goal of this paper is to provide a systematization of
knowledge for the computer science community. In doing so, we address some of
the (sometimes erroneous) beliefs of this field and we report on a survey we
conducted about genome data privacy with biomedical specialists. Then, after
characterizing the genome privacy problem, we review the state-of-the-art
regarding privacy attacks on genomic data and strategies for mitigating such
attacks, as well as contextualizing these attacks from the perspective of
medicine and public policy. This paper concludes with an enumeration of the
challenges for genome data privacy and presents a framework to systematize the
analysis of threats and the design of countermeasures as the field moves
forward
Tracking Report 2010 prAna, China 4000151034I
This document is part of a digital collection provided by the Martin P. Catherwood Library, ILR School, Cornell University, pertaining to the effects of globalization on the workplace worldwide. Special emphasis is placed on labor rights, working conditions, labor market changes, and union organizing.FLA_2010_prAna_TR_China_4000151034I.pdf: 16 downloads, before Oct. 1, 2020
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