- Code BIOL3204
- Unit Value 6 units
This course focuses on new discoveries in areas of importance to our understanding of human genetics and disease. Fuelled by Sequencing of the Human Genome and new methods of investigating biological function, research into the genetic and molecular causes of human disease is advancing at a rapid pace. We will examine not only the genetic abnormalities underlying human disease and disorders but also the breakdown in the physiological and molecular biology caused by the genetic lesion. We will also look at how this knowledge can lead to new treatments for some diseases and explore some of the societal issues raised by new technologies and treatments. We will cover topics including:
• genomic technologies and their application to human genetics
• the genetic basis of simple and complex traits
• animals models for human genetic diseases
• methods of gene expression control (genetic and epigenetic)
• potential disease treatments
• clinical genetics
On satisfying the requirements of this course, students will have the knowledge and skills to:
1. proficiently navigate relevant literature, web sites and databases for research into human genetics
2. describe the approaches used to identify the genetic basis of simple, heterogeneous and complex traits
3. describe the latest advances in genomic technologies and their application to personalised medicine
4. explain the importance of model species to our investigation of basic principles in human genetics.
5. explain how modern molecular techniques can be used in the diagnosis and treatment of cancer and inherited disease
6. describe the major types of mechanisms involved in regulating gene expression
7. identify some of the societal issues raised by new technologies and treatments
Assessment will examine proficiency in individual research, understanding of the theory and laboratory work. A sliding scale permits students to focus on areas of interest by designating the weight to be assigned to different items of assessment.
- Research essay (3000 word) on the current state of knowledge and recent advances in an area of human molecular genetics of specific interest to the student (25% to 45%) (1-7 depending on topic)
- Six short assignments on lecture and practical material (5% each) (LO1-7 depending on practical)
- Final examination to assess students’ understanding (25% to 45%) (LO2-7)
The ANU uses Turnitin to enhance student citation and referencing techniques, and to assess assignment submissions as a component of the University's approach to managing Academic Integrity. While the use of Turnitin is not mandatory, the ANU highly recommends Turnitin is used by both teaching staff and students. For additional information regarding Turnitin please visit the ANU Online website.
Two to three lectures per week and computer practicals; total workload ~ 45 contact hours in semester. In addition, the research essay requires substantial number of self-assigned (i.e. non-contact) hours.
Requisite and Incompatibility
Assumed KnowledgeBIOL2151 is strongly recommended.
Tuition fees are for the academic year indicated at the top of the page.
If you are a domestic graduate coursework or international student you will be required to pay tuition fees. Tuition fees are indexed annually. Further information for domestic and international students about tuition and other fees can be found at Fees.
- Student Contribution Band:
- Band 2
- Unit value:
- 6 units
If you are an undergraduate student and have been offered a Commonwealth supported place, your fees are set by the Australian Government for each course. At ANU 1 EFTSL is 48 units (normally 8 x 6-unit courses). You can find your student contribution amount for each course at Fees. Where there is a unit range displayed for this course, not all unit options below may be available.
Offerings and Dates
|Class number||Class start date||Last day to enrol||Census date||Class end date||Mode Of Delivery|
|2670||16 Feb 2015||06 Mar 2015||31 Mar 2015||29 May 2015||In Person|