Mini Map

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)

Offerings (1)

  • Second semesterClayton · ON-CAMPUS