Presentation: Find a genetic mutation causing your disease with Simple ClinVar

In 20 minutes, this open science database (web server) will be presented after being recommended by F1000Prime (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.  

There will be time for questions after the presentation.

For PhD students and researchers in pre-clinical and translational research. You must have and supply an email-address with the ending Register before 20 September.

Instructions: A link will be sent to all registered students one week before the workshop takes place; this link will enable you to enter the online classroom at the appointed time.

Language: English (but we do also speak Swedish). 

Tip! Click on Add to Calendar.

Questions? Contact Katarina Amcoff,

22 september
12:00 - 12:30
tisdag, 22 september, 2020 - 12:00