Unlock the power of Gene Set Enrichment Analysis with R at the GHGA summer school. Dive deep into functional interpretation of omics data. Practical workshops and expert guidance await. Apply now!
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Tudor Groza from the Agency for Science, Technology and Research (Singapore) will talk about "Towards automating the assembly of natural history of diseases" at the GHGA lecture series. Register now.
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We’re excited to co-organize the genomDE-Symposium 2025! Under the theme "Genomic Medicine. Seizing Opportunities. Helping People.", this event will bring together leading experts from clinics, research, policy, and medical informatics!
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Alex Wagner from the Nationwide Children's Hospital, Columbus, USA will talk about "The Variation Representation Specification (VRS) - enabling consistent variant exchange" at the GHGA lecture series. Register now!.
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Leslie Matalonga from the National Center for Genomic Analysis (CNAG), Barcelona will talk about "The Genome-Phenome Analysis Platform (GPAP) - A collaborative platform for diagnosis and gene discovery in rare disease research". Register now!
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This hands-on summer school introduces doctors, clinical staff, and medical researchers to the fundamentals of cloud technology and digital tools for handling sensitive data, using the de.NBI cloud.
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Save the date for the second Conference on Research Data Infrastructure in Aachen! Explore how better use of research data drives knowledge and benefits society, with keynotes, lectures, posters, and a market of opportunities.
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GA4GH 13th Plenary Meeting in Uppsala will bring together the global genomics and health community for workshops, presentations, and keynote talks that explore opportunities to scale genomic and clinical data sharing.
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Jean-Pierre Hubaux from the École polytechnique fédérale de Lausanne (EPFL) presented "GDPR-Compliant Federated Learning on Medical Data". Watch it now!
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GHGA organizes a satellite event at the conference 'Single Cell Omics in Clinical Applications' of the Single Cell Omics Germany network, taking place in Bonn.
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Sergi Beltran Agulló from the Centro Nacional de Análisis Genómico and Centre de Regulació Genòmica (CNAG-CRG) presented "Pan-European data sharing in Solve-RD contributes to diagnose Rare Diseases: can we make an even bigger impact?".
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Registration open - we are pleased to announce we have opened registration for the next internal GHGA Annual Meeting, 10-11 October 2022, in Tübingen.
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What is informed consent in research and medical settings? Why is it important and what are the challenges? To have these questions answered, tune in on our Webinar on 07 October 2022.
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William Rayner from the Helmholtz Munich presented "Genomic federated data analyses" on 26. September 2022, 16:00 (CET). Recording available.
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