- Code BIOL3205
- Unit Value 6 units
- Offered by John Curtin School of Medical Research
- ANU College ANU Joint Colleges of Science
- Course subject Biology
- Areas of interest Medical Science, Cell and Molecular Biology, Genetics, Biomedical Science
This course will extend on the Genetics of Human Disease I course, focussing on more advanced topics of human genetics and disease. We will examine the genetics of non-Mendelian disorders, including those exhibiting sex-linked, mitochondrial, transgenerational and complex modes of inheritance. These will be studied at both conceptual and disease-specific levels, with additional focus on the use of genetics to elucidate disease mechanism and develop therapies. We will also present the latest advances and representative examples pertaining to other advanced genetic concepts such as genome evolution, gene-environment interactions, and higher order genome organisation and regulation. We will cover topics including:
- Non-Mendelian inherited diseases.
- Complex trait genetics
- Gene-environment interactions
- Impact of disease on genome evolution
- Genetic approaches to treating disease
- Higher order genome structure and gene expression
Upon successful completion, students will have the knowledge and skills to:On satisfying the requirements of this course, students will have the knowledge and skills to:
- Proficiently locate and use web-based and literature-based resources to investigate hypotheses in the field of human genetics.
- Explain how genetic mutations cause disease in humans and relate this to the underlying physiological basis.
- Demonstrate how the genetic basis of complex genetic traits is determined.
- Describe how current and experimental-based therapies act to control and cure genetic diseases.
- Describe how interactions between environmental factors and genes influence disease phenotypes.
- Explain how selective pressure has affected the evolution of the human genome.
- Describe how phenotypic expression and disease can be determined by cis- and trans-acting DNA elements.
Indicative AssessmentAssessment will examine proficiency in individual research, understanding of the theory and practical work.
- 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 (30%) (LO 4-7 depending on topic)
- Take-home assignments that extend on lecturer-lead tutorials. Comprise of short answers relating to interpretation of prescribed research articles, or specific topics and questions set by the lecturer. (3 assignments, 10% each; total 30%) (LO 1-3)
- Final examination to assess students’ understanding (40%) (LO 2-7)
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WorkloadThree lectures per week and computer practicals; total workload ~ 45 contact hours in semester. In addition, the course requires substantial number of self-assigned (i.e. non-contact) hours.
Requisite and Incompatibility
Prescribed TextsHuman Molecular genetics 4th Edition Strachan and Read
Assumed KnowledgeBIOL2151 is strongly recommended.
Tuition fees are for the academic year indicated at the top of the page.
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- Student Contribution Band:
- 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, Dates and Class Summary Links
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Class summaries, if available, can be accessed by clicking on the View link for the relevant class number.
|Class number||Class start date||Last day to enrol||Census date||Class end date||Mode Of Delivery||Class Summary|
|9592||24 Jul 2017||31 Jul 2017||31 Aug 2017||27 Oct 2017||In Person||N/A|