Rami Abou Jamra from the University Leipzig will talk about "Genome sequencing for rare disease diagnostics: uncovering hidden causal variants" at the GHGA lecture series. Register now!
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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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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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The 5th Summer School of the Next Generation Sequencing Competence Network (NGS-CN) focuses on training young researchers in spatial transcriptomics and single-cell transcriptomics (hybrid & in-person in Dresden).
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The 11th ELIXIR All Hands Meeting will bring together members of the community from across the ELIXIR nodes and collaborators from partner organisations to review ELIXIR's recent achievements and activities, and to discuss future plans.
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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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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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Have heard of Galaxy - the open source, web-based platform for data intensive biomedical research? Tune in to our webinar to learn what it does, which tools it provides and how it can help your research!
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