cancelled! Join us for a captivating talk on the critical role of benchmarking and quality control in genomic variant calling.

Kyle Farh from Illumina will talk about "How do you train genomics AI?" at the GHGA lecture series. Register now!

Curious about Research Data Management (RDM) and its significance, especially in human research? de.NBI and GHGA have designed the ideal interactive training session for you, combining informative presentations with hands-on exercises!

Join the nf-core Hackathon to connect with fellow Nextflow and nf-core enthusiasts! Dive into three days of collaboration, coding, and innovation, tackling everything nf-core.

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.

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.

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.

Unlock the power of NGS harmonization! Join us for a two-part virtual webinar series on workflow standardization and benchmarking, featuring practical tips and best practices for achieving harmonization using the Sarek pipeline as an example.

This course is designed to provide an overview of data protection regulations and obligations, with a focus on the General Data Protection Regulation (GDPR).

Martin Hirst from the University of British Columbia (UBC) talked about "THe EpiATLAS – a reference for human epigenomic research". Watch it now!

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.

Struggling with interpreting statistical results? Join our next webinar on Interpretation of Results from Biostatistics.

Peter Robinson from The Jackson Laboratory (JAX), presented "The Phenopacket schema: an open standard for sharing disease and phenotype information". Watch it now!