The GHGA Lecture Series "Advances in Data-Driven Biomedicine" is a monthly virtual event series of scientific talks, presenting the fascinating world of data-driven medicine and their ethical, legal and social implications. We aim also to provide a platform for interactive discussion, so we encourage all participants to actively participate in the Q&A section after the lectures.
Invited guest lecturers are outstanding international researchers from different disciplines across omics data sciences. Selected on excellent academic merit and significant contributions to their respective fields, they actively shape international research agendas.
We invite you to join us monthly on Wednesdays from 16:00 to 17:00 (CET) via Zoom. All lectures are held in English, each lecture is free and open to everyone. Past lectures can be found in our GHGA YouTube Channel.
You can register for the whole lecture series here and never miss #GHGAtalks again!
We are very happy to receive feedback or ideas for further GHGA Lectures. Feel free to contact us using the contact form on this page or on Twitter.
Lorenz Grigull from the Center for Rare Diseases at the Bonn University Hospital will talk about "The Path to Diagnosis, Misdiagnoses, and Pattern Recognition in Medicine" at the GHGA lecture series. Register now!
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Steven Laurie from the Barcelona National Centre for Genomic Analysis (CNAG) will talk about "The RD-Connect Genome-Phenome Analysis Platform (GPAP)" at the GHGA lecture series. Register now!
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Sarah Teichmann from the Wellcome Trust Sanger Institute will talk about "(Machine) learnings for the Human Cell Atlas" at the GHGA lecture series. Register now!
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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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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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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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Jean-Pierre Hubaux from the École polytechnique fédérale de Lausanne (EPFL) presented "GDPR-Compliant Federated Learning on Medical Data". Watch it now!
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Sergi Beltran Agulló from the Centro Nacional de Análisis Genómico and Centre de Regulació Genòmica (CNAG-CRG) presented "Pan-European data sharing in Solve-RD contributes to diagnose Rare Diseases: can we make an even bigger impact?".
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William Rayner from the Helmholtz Munich presented "Genomic federated data analyses" on 26. September 2022, 16:00 (CET). Recording available.
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