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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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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In this webinar we will give you an introduction to what it takes to make data in this field Findable, Accessible, Interoperable and Reproducible - and how the FAIR principles can be implemented.
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New to single cell research? Looking for an introduction into scRNA sequencing and analysis workflows? Then look no more, we have a webinar for you.
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Marina DiStefano (Broad Institute) will present "The Gene Curation Coalition: A Global Effort to Harmonize Gene-Disease Evidence Resources". Watch it now!
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Are you planning large scale or high throughput laboratory experiments and are wondering which are the computational techniques and tools that help with efficient workflow design, data representation and computation? Then this webinar is for you.
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Metadata - everyone has heard the term, but what does it actually mean? And why are metadata important for research and data analysis? Answers to these questions will be given in the first part of this webinar. In the follow up we will tell you about the GHGA metadata ...
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