Tag: Rare Diseases Virtual Platform (VP)

Genetic Mapping

ERDERA unites 10 000 rare disease datasets in a single, secure European resource

In its first year, ERDERA has brought together 10 000 harmonised genomic and phenotypic datasets from unsolved rare disease cases across Europe, creating a secure, standardised and scalable resource.
FAIR Training Webinar ERDERA

Global audience joins FAIR Training Webinar to strengthen data practices in rare disease research

A successful training event with 350 registrations from 58 countries and daily attendance averaging 160 participants
Transforming Rare Disease Research in Europe

ERDERA: Transforming Rare Disease Research in Europe

ERDERA's

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