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 2026 in Semester 2 at Clayton. It needs BMS1062 and unlocks 9 units, leading on to 10 units in all.
- Credit points
- 6
- Offered in 2026
- Semester 2
- Clayton
- Assessment
- Exam 35%
- and 3 other tasks
- Workload
- 12 hours
- per semester
This is the 2026 handbook entry. See the 2027 entry.
Reviews
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Requisites
Before BMS2042
Prerequisites
Pass these before you enrol.
After BMS2042
9 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
- GEN3010Applied bioinformaticsNo 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
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)
Prerequisite: BMS1062
Prohibitions: GEN2041, GEN2052, GNA2042
Equivalent units
The same content under another code. Only one of them counts.
Overview
Offerings in 2026
| Teaching period | Campus | Mode |
|---|---|---|
| Second semester | Clayton | Blended |
Assessment
- In-semester applied scenario test (1.5 hours)Quiz / Test15%
- Case study (1,500 words)Written30%
- Team oral presentation (20-25 mins)Presentation20%
- Applied scenario examination (2 hours and 10 mins)Examination35%
Assessment details may change. Please refer to the assessment information in Moodle closer to the start of the teaching period.
Learning outcomes
When you finish this unit, you should be able to:
- 1
Apply your knowledge of genes, their inheritance and their interactions, to scenarios involving genetic disease, phenotypic variation and evolution.
- 2
Critically analyse tools commonly used in genetic research including molecular techniques and model organisms, propose relevant applications of them and contrast their strengths and weaknesses.
- 3
Analyse and interpret genetic observations and data using problem solving and mathematical skills.
- 4
Communicate genetic concepts, research and data to diverse audiences in a professional manner, in written and/or audio-visual formats as an individual and in teams.
- 5
Develop arguments that consider the ethical implications of genetic research and testing in public health.
Workload and teaching
- Assessments-
- Lectures24 hours
- Laboratories28 hours
An average of 6 hours of directed study per week, including 2 hours of lectures, 2.5 hours of lab and 1.5 hours of online activities.
An average of 6 hours per week of self-directed study.
Total per week = 12 hours.
Learning resources
Required resources
See Moodle for details about required resources.
Contacts
- Unit Coordinators
- Dr Hendrika Duivenvoorden
- Dr Callum Vidor
- Chief Examiners
- Dr Hendrika Duivenvoorden
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 9 units, including BCH3042, BMS3031, BMS3052, GEN3010, GEN3030 and GEN3040. Those lead on to 10 units in all.
When is BMS2042 offered?
In 2026, BMS2042 runs in Semester 2 at Clayton.
How much work is BMS2042?
The handbook expects about 12 hours of study across the semester. No students have rated its difficulty yet.
Does BMS2042 have an exam?
Yes. The exam is worth 35% of the final mark, alongside 3 other tasks.