MonMap
A course mapper by Monash Association of Coding (MAC)
Genome curation
GNA5120
Synopsis
The use of genome scale data in clinical applications is rapidly increasing. You will develop expertise in the use of software applications for the calling of genome sequence variants. You will learn how to interpret these variants including examining their presence in population datasets and clinical scenarios.
You will learn about population stratification and ethnic specific variation; how to apply this knowledge to the interpretation of genome sequences, and the use of genomics in precision medicine.
Sourced from the Monash Handbook 2026.
Quick facts
- Credit points
- 12
- Level
- 5
- Audience
- Postgraduate
- Type
- Coursework
- School
- Faculty of Science
- Faculty
- School of Biological Sciences
- Handbook year
- 2026
Prerequisites (1)
What it unlocks (3)
- Cancer genomicsGNA5042
- Advanced case studies in genomicsGNA5920
- Genomics internshipGNA5930
Offerings (1)
- Second semesterClayton · ON-CAMPUS