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Presentations and flyers

Presentations and flyers

Download posters, presentations and communication materials

RD-Connect Flyers

Genome-Phenome Analysis Platform

Registry & Biobank Finder

Sample Catalogue

FP7 Success Story

Presentations

Cross-cutting bottlenecks and solutions in rare disease research

RD-Connect summary slide

A paradigm for best practice in data sharing in genomic studies

Annual Meeting 16th - 18th May 2018 - Athens, Greece

Work package updates and Patient Involvement session

WP2 update: Rare disease patient registries

WP3 update: Rare disease biobanks

WP4 update: Bioinformatic tools

WP5 update: Genome-Phenome Analysis Platform

WP6 update: Ethical, Legal and Social Issues

WP7 update: Impact

WP8 update: Patient engagement

Pauline MacCormack - Why Patient Involvement?

Annual Meeting 1st - 2nd May 2017 - Berlin, Germany

Main Achievements and Challenges

WP4 Bioinformatics Tools

WP8 Patient Engagement

Cross-Cutting Session - Biobanks and Biosamples

Biobanks and biosamples

Cross-Cutting Session - Platform Development and Tools

BBMRI -LPC (WP5) – Preliminary results

Multi-Omics analysis

WP4 cross-cutting session

Platform and tools cross-cutting session

Data Linkage Plan and Privacy Protecting Record Linkage (PPRL)

The rare disease data linkage plan

FAIR data principles for cross-resource questions in European Reference Networks

Ethical, Legal and Social Issues (ELSI)

ELSI cross-cutting session/BBMRI initiative for a Code of Conduct

Posters

RD-Connect: an integrated infrastructure for data sharing and analysis in rare disease research (ECRD 2018)

RD-Connect: an FP7 success story (April 2018)

Webinar slides

Linking up all those data: why should we make data FAIR (Marco Roos, 26/09/2018)

Finding registries and biosamples in just a few clicks: RD-Connect Registry & Biobank Finder and Sample Catalogue (Mary Wang, 18/09/2018)

EuroBioBank webinar - What is BBMRI-ERIC (slides from the webinar on 16/07/2018)

EuroBioBank webinar - BBMRI Rare Diseases Working Group (slides from the webinar on 16/07/2018)

Webinar for biobankers: Sample Catalogue - browsing data (Mary Wang, 24/01/2018)

Webinar for biobankers: Sample Catalogue - uploading sample data (David van Enckevort, 24/01/2018)

How to Promote Data Sharing in Rare Disease while Protecting Privacy (Mats Hansson)

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