Skip To Content
Practical Medical Genomics is a Course

Practical Medical Genomics

Oct 17, 2022 - Dec 19, 2022
3 credits

$2,000 Enrol

Full course description

 

 

 

 

Start

17 October 2022

Duration

40 hours
(2 months)

Delivery Mode

Online
(asynchronous &
synchronous)

Price

$2,000.00
(GST inclusive)

15% Discount^

Use promo code
SC15OFF

 

 

 

 

Through the progression of this course, you will be introduced to the practical aspects of genetic and genomic testing; the many technologies involved; and the challenges around successful integration of genomics into clinical practice. We will also explore the likely future trends in this rapidly changing field of research driven clinical practice. At the end of this course, participants will be equipped with the tools, knowledge and insight required to integrate genomics into their practice and understand how genomic medicine fits into healthcare in Australia.

This course builds on the experience and expertise of UNSW Medicine and Health and UNSW Science, plus that of Garvan’s Kinghorn Centre for Clinical Genomics. The credential short course aligns with curricula of relevant medical colleges and professional societies (such as RACP, RACGP, RCPA and HGSA).

What are the course learning outcomes?

By the end of this course, you will be able to:

  • Identify when to consider genetic and or genomic testing to achieve the best healthcare outcomes.
  • Interpret genetic/genomic test result reports.
  • Integrate understanding of genetic and genomic concepts into best practice when communicating with peers and patients pre- and post- testing, including when obtaining informed consent for testing and discussing genetic/genomic test results.
  • Synthesise knowledge gained in the course to develop evidence-based care plans that are patient and family-centred and appropriately involve patient support groups and interdisciplinary teams.

What core topics are offered?

The following topics are offered in the course for developing and increasing your knowledge, understanding and skills in practical medical genomics.

  • Delivering person-centred care in genomics
  • Eliciting and interpreting family health history
  • Communicating genomic concepts
  • Facilitating shared decision-making in genomic medicine
  • Ordering and using genomic tests
  • Interpreting genomic test results
  • Communicating results
  • Seeking information and coordinating care
  • Linking to holistic family-centred supports
  • Medicolegal, ethical and cultural considerations in genomics

Who is this course suited to?

Health and science professionals who are interested in learning more about genomics. This applies to both people who are currently applying genomics in their practice, as well as those who are interested in applying genomics in the future. Participants may include paediatricians, medical specialists, registrars, other doctors-in-training, allied health professionals, nurses, researchers and laboratory scientists.

Virtual Sessions

  • Welcome session: 17 October 2022 | 6:00 pm - 7:00 pm
  • Case based workshops (Compulsory attendance): 19 November 2022 | 9:00 am - 4:30 pm
  • Group presentations and wrap up (Compulsory attendance): 3 December 2022 | 9:00 am - 1:00 pm
  • Compulsory final assessment due date: 19 December 2022

What are the course credentials?

This course is worth 3 UNSW Medicine & Health Executive Certificate in Health (FMECH) points, which provides formal recognition of professional development and reflects 40 hours of learning inclusive of pre-work, course participation, learning materials and support. Upon course completion, you will be issued with a UNSW Medicine & Health verifiable credential.

The credential is valid for 3 years and may be counted towards your continuing professional development (CPD). Please check with your college as the credential provides documentary evidence which may substantiate activities claimed under your college program. 

 

Can I use my credit towards further study?

There is an additional assessment associated with this course. All participants will be issued with 3 FMECH points upon completion of the course and the compulsory formative assessment, but it is essential to complete the additional assessment if you wish to apply to use the points towards credit for a UNSW postgraduate program in the future.

Inclusions

Price is inclusive of 40 hours of learning, digital badging, online credential learning resources, evidence-based research, practical tools and techniques, support and course completion assessment.

Discounts

^15% discount for UNSW Network, Affiliates, Staff, Students, Adjuncts, and Partners.

Presenters



Dr Elizabeth Emma Palmer
FRACP, PhD, MBBS, BA, AFHEA


Emma Palmer is a clinical academic working as a Clinical Geneticist at Sydney Children’s Hospital Network (SCHN), Randwick, and Lecturer at the University of New South Wales. Emma has extensive teaching experience at both the pre and post graduate level and has developed resources on genomic education for clinicians and patients as part of national and international collaborations.

 


Dr Emily Oates
FRACP, PhD, MBBS, BMedSc


Emily Oates is a Clinical Geneticist, an honorary Sydney Children’s Hospital Network staff specialist and an NHMRC Research Fellow. Dr Oates also convenes the UNSW 3rd year Human Molecular Genetics course (BAB3151), recently led development of a new genetics/genomics campus day for senior UNSW medical students and is contributing to the development of a genetics-focused General Education course.

 

Further information

Thank you for considering UNSW Medicine & Health Short Courses. Reach us for further information about this short course. Or drop us a line if you would like to receive future short courses for early bird discounts.

We continuously improve our short courses to reflect the needs of our learners and their employers. If you are interested in connecting with us to explore bespoke programs for your organisation or team, please contact us.