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This unit caters for practitioners, policy and decision-makers, students and researchers in public health, public policy, journalism, law, epidemiology, medicine, science, industry, ethics, philosophy, screening, communication and advocacy. It gives a basic introduction to concepts in genetics and genomics, and covers real-life examples of how genetics and genomics is used in health settings including genomics for COVID-19 control, genomic testing and screening for cancer, familial hypercholesterolemia, newborns, community settings, and in outbreak investigations. It covers epidemiological, psychosocial, legal, ethical, education and policy aspects of genomic testing, and genetic determinants of disease.
Study level | Postgraduate |
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Academic unit | Public Health |
Credit points | 6 |
Prerequisites:
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PUBH5010 or CEPI5100 |
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Corequisites:
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None |
Prohibitions:
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None |
Assumed knowledge:
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Basic epidemiology No previous knowledge of genetics is required |
At the completion of this unit, you should be able to:
This section lists the session, attendance modes and locations the unit is available in. There is a unit outline for each of the unit availabilities, which gives you information about the unit including assessment details and a schedule of weekly activities.
The outline is published 2 weeks before the first day of teaching. You can look at previous outlines for a guide to the details of a unit.
Session | MoA ? | Location | Outline ? |
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Intensive October 2021
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Block mode | Camperdown/Darlington, Sydney |
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