Earners of this credential can describe cellular hallmarks of cancer and how gene variants contribute to cancer development. Earners can interpret genomic tumor testing reports, describe types of genomic variants detected using genomic sequencing, and distinguish between germline and somatic variants. Earners can discuss how genomic tumor testing is used in precision medicine and how the presence of clinically significant gene variants can lead to personalized treatment plans for some patients.

• Type Learning
• Level Foundational
• Time Weeks
• Cost N/A