Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Precision Oncology: Genomics Guided Care - How to Prepare and Read Genomics Reports for Clinical Practice?

Aired live on 14 Feb 2024

ESMO-Webinar-series-Genomics-Clinical-Practice-1000x250

Precision Oncology: Genomics Guided Care - How to Prepare and Read Genomics Reports for Clinical Practice?

Chair: Joaquin Mateo
Speakers: Joris van der Haar, Debyani Chakravarty, Clare Turnbull

ESMO-Webinar-series-Genomics-Clinical-Practice-1000x250

Login to get immediate access to this content.

Login

Learning objectives:

  • Increase knowledge in how to read and interpret clinically oriented genomics reports.
  • Learn how to interpret “functional impact" and "clinical relevance" of classification systems for mutations in genomics reports.
  • Discuss indications of secondary germline testing based on reports from tumour-only genomics tests.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.