Genetics forms the nexus between human biology and the environment with almost every human disease having a genetic component. This course covers the basic tenets of human genetics, introducing genetic concepts and building on these throughout the course. This will lead through discussions on: cytogenetics and chromosome disorders, Mendelian diseases, and the genetic complexity of some common human diseases. The role of the human genome and ongoing variation mapping projects, in our current understanding of genetic disease will also be introduced with the statistical and technological base of genetics and genomics being discussed. Specialist topics will also be explored including cancer genetics, bioinformatics and genetic counselling. Key concepts that will be covered include: segregation, linkage and linkage disequilibrium, genetic association and their application to population and family based genetic studies.
|Unit name||Human Genetics|
|College/School||College of Health and Medicine
School of Medicine
|Discipline||Medicine|Menzies Institute for Medical Research|
|Coordinator||Professor Graeme Zosky|
|Available as student elective?||Yes|
|Location||Study period||Attendance options||Available to|
- International students
- Domestic students
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|Study Period||Start date||Census date||WW date||End date|
* The Final WW Date is the final date from which you can withdraw from the unit without academic penalty, however you will still incur a financial liability (see withdrawal dates explained for more information).
Unit census dates currently displaying for 2022 are indicative and subject to change. Finalised census dates for 2022 will be available from the 1st October 2021.
- Explain complex genetic concepts and be able to apply these concepts to explain the genetic basis of human traits, including disease
- Critically evaluate research literature related to the genetic basis of human traits including disease
- Explore the ethical principles of genetic research and the use of genetic information in society
- Use modern approaches, including statistics and bioinformatics, to measure and interpret genetic data such as genetic variation between individuals
|Field of Education||Commencing Student Contribution 1||Grandfathered Student Contribution 1||Approved Pathway Course Student Contribution 2||Domestic Full Fee|
1 Please refer here more information on student contribution amounts.
2 Information on eligibility and Approved Pathway courses can be found here
If you have any questions in relation to the fees, please contact UConnect or more information is available on StudyAssist.
Please note: international students should refer to this page to get an indicative course cost.
PrerequisitesCBA265 AND (CZZ101 OR KPZ164)
2 x 1 hr lectures and 1 x 1 hr tutorial per week
|Assessment||Four quizzes (20%)|Final exam (40%)|Written Essay (20%)|Ethics reflection (10%)|Statistics/Bioinformatics assignment (10%)|
|Timetable||View the lecture timetable | View the full unit timetable|
Required readings will be listed in the unit outline prior to the start of classes.
|Links||Booktopia textbook finder|
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