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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Martin Hirst from the University of British Columbia (UBC) talked about "THe EpiATLAS – a reference for human epigenomic research". Watch it now!
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New to the field of epigenetics and its analysis methods? Or just looking for a brief intro to the topic? Then we have a webinar for you - in ‘A Beginners Guide to Epigenetics’ we will talk about the basics of epigenetic research and analysis methods.
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Struggling with interpreting statistical results? Join our next webinar on Interpretation of Results from Biostatistics.
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Peter Robinson from The Jackson Laboratory (JAX), presented "The Phenopacket schema: an open standard for sharing disease and phenotype information". Watch it now!
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GHGA is going to participate at the GfH conference (German Society for Human Genetics) and will organize a workshop titled “The German Human Genome-Phenome Archive (GHGA): Best practice examples for shared genome data usage”.
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Christoph Schickhardt from the National Center for Tumor Diseases Heidelberg (NTC) will talk about "A standardized broad consent for long-term secondary use of health data and biosamples". Watch it now!
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