Peter Robinson from The Jackson Laboratory (JAX), will talk about "The Phenopacket schema: an open standard for sharing disease and phenotype information". Register now!
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It is our pleasure to announce that the GHGA Annual Meeting 2023 will take place 04.-05. October in Heidelberg.
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Join the Next Generation Sequencing Competence Network Workshop 2023 to learn state-of-the-art NGS technologies and data analysis for various areas of life sciences and exchange with fellow researchers.
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The ELIXIR All Hands 2023 brings together members of the community from across the ELIXIR Nodes, and collaborators from partner organisations, in order to review ELIXIR’s achievements and activities so far and discuss plans for the future.
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CSAMA 2023 is a one week intensive course on Statistical Data Analysis for Genome-Scale Biology and teaches statistical and computational data analysis of multi-omics studies in biology and biomedicine.
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Bring together researchers and scientists, along with software engineers and Science Gateways developers, this workshop will discuss problems and solutions in the area, and push towards the wider adoption of Science Gateways in e-Science.
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Under the theme Connecting Communities, the NFDI and KIT are inviting national and international stakeholders from all research fields as well as from the infrastructure sector to present their contributions to an excellent research data management of the future.
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EuroBioC is the European Conference for Bioconductor, an open-source community and a non-profit organization that develops some of the most widely used data analysis tools in bioinformatics.
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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". Recording available.
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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". Recording available.
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