BMS2042 Human genetics
Faculty of Medicine, Nursing and Health Sciences
BMS2042 Human genetics is a level 2, 6-credit-point, undergraduate unit from the Faculty of Medicine, Nursing and Health Sciences, offered in 2022 in Semester 2 at Clayton. It needs BMS1062 and unlocks 8 units, leading on to 10 units in all.
- Credit points
- 6
- Offered in 2022
- Semester 2
- Clayton
- Assessment
- Exam 45%
- and 3 other tasks
This is the 2022 handbook entry. See the 2027 entry.
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Requisites
Before BMS2042
Prerequisites
Pass these before you enrol.
Prohibitions
You can't enrol if you have passed any of these.
After BMS2042
8 units list BMS2042 as a prerequisite or corequisite.
- BCH3042Cell signal transduction: Role in cancer and human diseaseNo reviews yet
- BMS3031Molecular mechanisms of diseaseNo reviews yet
- BMS3052Biomedical basis and epidemiology of human diseaseNo reviews yet
- GEN3030Molecular, cellular and developmental geneticsNo reviews yet
- GEN3040Genomics and its applicationsNo reviews yet
- GEN3051Medical and forensic geneticsNo reviews yet
- GEN3062Evolutionary and ecological geneticsNo reviews yet
- GEN3990Genetics in action research projectNo reviews yet
Enrolment rules
Corequisite: Must be enrolled in one of the following:
- Bachelor of Biomedical Science (including double degree programs)
- Bachelor of Biomedical Science (Scholar Program)
- Bachelor of Biomedical Science Advanced with Honours
Equivalent units
The same content under another code. Only one of them counts.
Overview
Offerings in 2022
| Teaching period | Campus | Mode |
|---|---|---|
| Second semester | Clayton | On campus |
Assessment
- Weekly practicals30%
- Short answer practical test15%
- Independent project10%
- Examination (2 hours and 10 minutes)Threshold hurdle45%
Learning outcomes
When you finish this unit, you should be able to:
- 1
Explain the central role of genes in the inheritance of traits and the complex variation in inheritance patterns that arise due to interactions of genes with each other and the environment;
- 2
Explain how genetic variation is generated by mutation and the importance of this in phenotypic variation, evolution and disease;
- 3
Describe the value of model organisms in studying human gene function in development and disease;
- 4
Demonstrate understanding of the relevance and value of genetics to human society;
- 5
Demonstrate skills in independent problem-solving and experimental design, and in data collection, analysis and interpretation;
- 6
Demonstrate skills in written and oral communication through written reports and oral presentations of research findings by small groups.
Workload and teaching
- Lectures24 hours
- Laboratories21 hours
The workload to achieve the learning outcomes for this unit is 144 hours spread across the semester (roughly 12 hours per week) - approximately an even mixture of attendance at scheduled activities and self-scheduled study time. Learning activities comprise a mixture of instructor directed, peer directed and self-directed learning, which includes face-to-face and online engagement.
Learning resources
Required resources
See Moodle for details about required resources.
Contacts
- Unit Coordinators
- Dr Hendrika Duivenvoorden
- Mr Callum Vidor
- Chief Examiners
- Dr Richard Burke
Common questions
What are the prerequisites for BMS2042?
You need BMS1062 before you enrol. Enrolment rules also apply.
What can I take after BMS2042?
BMS2042 is a prerequisite or corequisite for 8 units, including BCH3042, BMS3031, BMS3052, GEN3030, GEN3040 and GEN3051. Those lead on to 10 units in all.
When is BMS2042 offered?
In 2022, BMS2042 runs in Semester 2 at Clayton.
Does BMS2042 have an exam?
Yes. The exam is worth 45% of the final mark, alongside 3 other tasks.