RD-Connect links up rare disease research internationally to create an integrated hub enabling researchers to share rare disease research results and omics data.
http://www.rd-connect.eu/
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RD-CONNECT | An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research | rd-connect.eu Reviews
https://rd-connect.eu
RD-Connect links up rare disease research internationally to create an integrated hub enabling researchers to share rare disease research results and omics data.
Welcome - RD-Connect
Makes your Registry / Biobank visible. The RD Connect Network. Linking up rare disease resarch across the world.
RD-Connect Dataportal
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. Welcome to the central platform for access to data submitted by RD-Connect’s partner projects. The online genomics analysis interface is currently only open to beta-testers, but we look forward to welcoming additional users later in 2015. Please email platform@rd-connect.eu. To register for updates on platform release. If you want to be notified when registration opens. The biosample c...
rd-connect.eu
Bioinformatics tools | RD-CONNECT
http://rd-connect.eu/platform/bioinformatics-tools
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms Definitions. Collaborating & Contributing Projects. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). The multitude of...
Newsletters | RD-CONNECT
http://rd-connect.eu/newsletters
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms Definitions. Collaborating & Contributing Projects. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). RD-Connect issue...
Events for September 2016 | RD-CONNECT
http://rd-connect.eu/events/month
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms Definitions. Collaborating & Contributing Projects. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). Summer School an...
Upcoming Events Events | RD-CONNECT
http://rd-connect.eu/events
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms Definitions. Collaborating & Contributing Projects. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). Istituto Superio...
About RD-Connect | RD-CONNECT
http://rd-connect.eu/about
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms Definitions. Collaborating & Contributing Projects. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). RD-Connect is a ...
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Cooperation to European projects & partnerships with laboratories
http://www.interactive-biosoftware.com/genetic-software-company/projects
Interactive Biosoftware actively participates in European projects. Will develop a global infrastructure for sharing the research outputs of these and other rare disease projects, enabling scientists and clinicians worldwide to access a single centralized repository for omics data, phenotypic and biomaterial information. Learn more about RD-Connect in the News section. Learn more about BRIDGES here. PROF MILAN MACEK Jr. M.D. Ph.D. Charles University, Prague. Variant Effect Prediction Training Course.
Care and Trial Site Registry
https://ctsr.uniklinik-freiburg.de/passwordforgotten;jsessionid=0669581CAE3B5FAB42DE102E533F4DD3
Please enter your email address to request a new password. After clicking the 'Request new password' button you should receive an email containing your new password. If you have any questions, please contact us at ctsr@uniklinik-freiburg.de. Medical Center - University of Freiburg T: 49 761 270-44970 E: ctsr-info@uniklinik-freiburg.de. Mathildenstr. 1, 79106 Freiburg, Germany. Would you like to save your changes?
Pages - Home
https://spainrdr.isciii.es/Paginas/VariationRoot.aspx
Turn on more accessible mode. Turn off more accessible mode. Skip to main content. SpainRDR - Data and Reports. Welcome to the SpainRDR website. The Spanish Rare Diseases Registries Research Network-SpainRDR. Is a project financed by the Institute of Health Carlos III (ISCIII) within the scope of the IRDiRC for the years 2012 to 2014 with 2.4 M . 160; . 160; . 160;The International Rare Diseases Research Consortium. EUROPEAN PLATFORM FOR RARE DISEASES REGISTRIES . 160; GLOBAL RARE DI...
Links | SPATAX Network : Clinical and Genetic Analysis of Spastic paraplegia and Ataxia
https://spatax.wordpress.com/links
SPATAX Network : Clinical and Genetic Analysis of Spastic paraplegia and Ataxia. Https:/ spatax.wordpress.com. Association Paraplégie Spastique Héréditaire et Nos Enfants. Association Française de l’Ataxie de Friedreich (AFAF). Association Connaître les Syndromes Cérébelleux Association (CSC). Association Strümpell-Lorrain Association Strümpell-Lorrain (ASL). Centre National de la Recherche Scientifique (CNRS). Ecole Pratique des Hautes Etudes (EPHE). The EPHE neurogenetics team website.
Consortium
http://www.eurenomics.eu/the-group/consortium
Heidelberg University Medical Center. Institut national de la santé et de la recherche médicale (INSERM). Istituto di Ricerche Farmacologiche Mario Negri. University Medical Centre Utrecht. Radboud University Nijmegen Medical Centre. University College London - Centre for Nephrology. Agencia Estatal Consejo Superior de Investigaciones Científicas. University of Newcastle upon Tyne. Assistance Publique - Hôpitaux de Paris. University of Oulu - Biocenter. Philogen S.p.A. Project Coordinator / Project Office.
Projects | UA.PT Bioinformatics
http://bioinformatics.ua.pt/projects
Universidade de Aveiro, DETI / IEETA. 3810-193 Aveiro, Portugal. Jlo( at )ua.pt. 351) 234 370 500. EMIF – European Medical Information Framework. This project combines the topic of generating a common patient health Information Framework (IF) with addressing the two Research Topics (RT’s) Obesity and its metabolic complications and Markers for the development of Alzheimer’s disease (AD) and other dementias. Feb2013 – Dec.2014. NeuroPath – New Strategies Applied to Neuropathological Disorders. Implementat...
TREAT-NMD : TACT : TREAT-NMD Advisory Committee for Therapeutics
http://www.treat-nmd.eu/tact
All about the network. Network Chair and Vice-Chair. About the TREAT-NMD network. Donate to the TREAT-NMD Alliance. Nominations for Executive Committee members. Draft of EU data protection regulation. Meetings and events calendar. Submit a newsletter article. Cookies and privacy policy. Neuromuscular care and trial centres. Care and trial site registry. What is a patient registry? List of registries by disease. Principles of a review. Future meetings and events. NMR (MRI and MRS). Why use the BioBank?
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RD-CONNECT | An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research
An integrated platform connecting databases, registries, biobanks and clinical bioinformatics for rare disease research. An introduction from the coordinator. Glossary of Terms – Definitions. Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Global platform for data exchange. Ethics, legal and social issues. Sharing bio-specimens and data. Standards for informed consent. Rare Disease Patient and Ethics Council (RD-PEC). Patient Advisory Council (PAC). Databases and patient registries.
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