Experiment scenarios, prototypes and report - Iteration 1

The task of WP6 is to evaluate the CONNECT technologies under realistic situations. To achieve this goal, WP6 concentrated its effort in the development of a main scenario in the context of the GMES, which required the connection of two very different and independently build systems provided by the industry partners. The first one is a video-surveillance system provided by Thales; the second one, is an implementation of the GSMA Rich Communication Suite provided by DOCOMO. The resulting scenario allows to verify the validity of some of the CONNECT claims and to investigate with the introduction of some of the CONNECT technologies in the context of the integration of real systems. In addition, WP6 started the work of evaluating how the overall CONNECT work cycle can be introduced in the context of industrial prototype development

Initial CONNECT Architecture

Interoperability remains a fundamental challenge when connecting heterogeneous systems which encounter and spontaneously communicate with one another in pervasive computing environments. This challenge is exasperated by the highly heterogeneous technologies employed by each of the interacting parties, i.e., in terms of hardware, operating system, middleware protocols, and application protocols. The key aim of the CONNECT project is to drop this heterogeneity barrier and achieve universal interoperability. Here we report on the development of the overall CONNECT architecture that will underpin this solution; in this respect, we present the following contributions: i) an elicitation of interoperability requirements from a set of pervasive computing scenarios, ii) a survey of existing solutions to interoperability, iii) an initial view of the CONNECT architecture, and iv) a series of experiments to provide initial validation of the architecture

Experiment Scenarios

The scenarios proposed in this deliverable are intended to identify the multiple dimensions of interoperability, and also foster further discussions with other work packages (WP1 to WP5). These will be refined and extended as the project progresses. The scenarios have been grouped into three computing domains: Ubiquitous computing, Daily life support and Telco Web 2.0 & Cloud Computing. Although the scenarios are partitioned into domains, they all have common properties such as the presence of disparate devices, a large proportion of peer-to-peer traffic and disparate interaction patterns

The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia:

BACKGROUND: The c.429_452dup24 of the ARX gene is a rare genetic anomaly, leading to X-Linked Intellectual Disability without brain malformation. While in certain cases c.429_452dup24 has been associated with specific clinical patterns such as Partington syndrome, the consequence of this mutation has been also often classified as "non-specific Intellectual Disability". The present work aims at a more precise description of the clinical features linked to the c.429_452dup24 mutation. METHODS: We clinically reviewed all affected patients identified in France over a five-year period, i.e. 27 patients from 12 different families. Detailed cognitive, behavioural, and motor evaluation, as well as standardized videotaped assessments of oro-lingual and gestural praxis, were performed. In a sub-group of 13 ARX patients, kinematic and MRI studies were further accomplished to better characterize the motor impairment prevalent in the ARX patients group. To ensure that data were specific to the ARX gene mutation and did not result from low-cognitive functioning per se, a group of 27 age- and IQ-matched Down syndrome patients served as control. RESULTS: Neuropsychological and motor assessment indicated that the c.429_452dup24 mutation constitutes a recognizable clinical syndrome: ARX patients exhibiting Intellectual Disability, without primary motor impairment, but with a very specific upper limb distal motor apraxia associated with a pathognomonic hand-grip. Patients affected with the so-called Partington syndrome, which involves major hand dystonia and orolingual apraxia, exhibit the most severe symptoms of the disorder. The particular "reach and grip" impairment which was observed in all ARX patients, but not in Down syndrome patients, was further characterized by the kinematic data: (i) loss of preference for the index finger when gripping an object, (ii) major impairment of fourth finger deftness, and (iii) a lack of pronation movements. This lack of distal movement coordination exhibited by ARX patients is associated with the loss of independent digital dexterity and is similar to the distortion of individual finger movements and posture observed in Limb Kinetic Apraxia. CONCLUSION: These findings suggest that the ARX c.429_452dup24 mutation may be a developmental model for Limb Kinetic Apraxia

Towards an architecture for runtime interoperability

Interoperability remains a fundamental challenge when connecting heterogeneous systems which encounter and spontaneously communicate with one another in pervasive computing environments. This challenge is exasperated by the highly heterogeneous technologies employed by each of the interacting parties, i.e., in terms of hardware, operating system, middleware protocols, and application protocols. This paper introduces Connect, a software framework which aims to resolve this interoperability challenge in a fundamentally different way. Connect dynamically discovers information about the running systems, uses learning to build a richer view of a system's behaviour and then uses synthesis techniques to generate a connector to achieve interoperability between heterogeneous systems. Here, we introduce the key elements of Connect and describe its application to a distributed marketplace application involving heterogeneous technologies

10 | Beni Isguen – Bouzeis

Ouvrage publié avec le concours et sur la recommandation du Conseil international de la philosophie et des sciences humaines (UNESCO). Ce volume, à l'origine publié par Edisud, est désormais diffusé par les Editions Peeters sous l'Isbn : 978-2-85744-549-4

10 | Beni Isguen – Bouzeis

Ouvrage publié avec le concours et sur la recommandation du Conseil international de la philosophie et des sciences humaines (UNESCO). Ce volume, à l'origine publié par Edisud, est désormais diffusé par les Editions Peeters sous l'Isbn : 978-2-85744-549-4

3 | Ahaggar – Alī ben Ghaniya

Ouvrage publié avec le concours et sur la recommandation du Conseil international de la philosophie et des sciences humaines (UNESCO). Ce volume, à l'origine publié par Edisud, est désormais diffusé par les Editions Peeters sous l'Isbn : 978-2-85744-260-8