Presentation: Find a genetic mutation causing disease with Simple ClinVar

In 30 minutes, this open science database (web server) will be presented after being recommended by F1000Opinions (in June 2019). Simple ClinVar allows for an easier and more intuitive visualization of the data in ClinVar (the largest publically available genetic variant database) and can be used on mobile devices.

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There will be time for questions after the presentation. 

This presentation is for doctoral students and researchers in clinical or translational research. It is held in English but we also speak Swedish.

The presentation is free but you need to register. 

Please note

A link will be sent to all registered participants the day before the event; this link will enable you to enter the online classroom at the appointed time. To maintain the best possible quality of our workshops, we have a limited number of participants – please make sure you unsubscribe if you can't make it! Your registration is handled in our booking system where you also unsubscribe. In case of too few participants, we reserve the right to cancel the event.


Anja Vikingson