28-29 November 2024

Melbourne Brain Centre Auditorium, Kenneth Myer Building,

30 Royal Parade, Parkville, VIC 3052

On behalf of the Organising Committee, we invite you to the 4th Australian Functional Genomics Symposium, to be held over 2 sessions on 28th and 29th of November.

Over the two days, we will bring together the clinical community involved in disease gene discovery and Australian research groups using a diverse array of disease model systems for the characterisation of genetic variants.

Invited speakers will showcase the increasing need to facilitate the clinical interpretation of genetic variants and how Australian functional genomics researchers can help. By combining the diverse knowledge of many aspects of genomic and functional interpretation, we hope to draw out critical discussion and novel approaches to understanding human genomic variation. This is of crucial importance to enable the translation of genomic findings into a patient diagnosis.

Key dates

Early bird registration closes: 25 October 2024

Final chance to register: 22 November 2024

Program overview

Invited speakers will present on current and emerging approaches to functional investigations across a variety of disease areas as well as insights into translation into the diagnostic pipeline.

We are proud to announce the following speakers who will present in our program:

Anai Gonzalez (CMRI); Andy Ng (UNSW); Avnika Ruparelia (UoM); David Ascher (UQ); Hamish Scott (SA Path); Ian Smyth (Monash); Lachlan Jolly (Adelaide Uni); Natasha Harvey (UniSA); Rehan Villiani (QIMR); Sally Dunwoodie (VCCRI); Sandra Cooper (Usyd); Zornitza Stark (VCGS)

The AFGN will be hosting a social event at the Science Gallery Melbourne on the Thursday evening of the Symposium.

Session times

Day 1 – Thursday 28/11
Session

Start Time

End Time

Duration

Arrival

9:30 AM

10:00 AM

0:30

Session 1 10:00 AM 12:00 PM

2:00

Lunch

12:00 PM

12:30 PM

0:30

Poster Session A

12:30 PM

1:00 PM

0:30

Session 2

1:00 PM

2:55 PM

1:55

Afternoon Tea

2:55 PM

3:25 PM

0:30

Session 3

3:25 PM

4:50 PM

1:25

 

Social Event @ Science Gallery

 

6:00 PM

 

9:00 PM

 

3:00

 

Day 2 – Friday 29/11
Session

Start Time

End Time

Duration

Arrival

8:45 AM

9:00 AM

0:15

Session 4

9:00 AM

10:40 AM

1:40

Morning Tea

10:40 AM

11:10 AM

0:30

Session 5

11:10 AM

1:00 PM

1:30

Lunch

1:00 PM

1:30 PM

0:30

Poster Session B

1:30 PM

2:00 PM

0:30

Session 6

2:00 PM

3:50 PM

1:50

Closing address

3:50 PM

4:05PM

0:15

 

Registration

Follow the link to our registration page to secure your ticket to the Symposium.

Early bird registration closes on October 25th 2024.

Abstract submissions

Abstract submissions closed on September 13th 2024.

Authors of accepted abstracts will be notified in early October.

Getting there

The Melbourne Brain Centre is located on the University of Melbourne Parkville campus in the Kenneth Myer Building. The auditorium is on the ground floor across. Use the main entrance, next to Dr Dax café, to access the auditorium foyer.

 

Accommodation

The Melbourne Brain Centre is located in Parkville, Melbourne with accommodation available nearby and in the surrounding suburbs, including Carlton, North Melbourne.

The venue is also easily accessible from Melbourne CBD.

Suggestions are listed in order of proximity:

  1. Mercure North Melbourne | Corner Flemington Road & Harker Street, North Melbourne, 3051 Melbourne, Australia
  2. The Larwill Studio | 48 Flemington Road, 3052 Melbourne, Australia
  3. City Edge North Melbourne Apartment Hotel | 188 Peel Street, North Melbourne, 3051 Melbourne, Australia 
  4. Best Western Queen Victoria Market Hotel | 77 – 79 Capel Street, West Melbourne, 3003 Melbourne, Australia
  5. ibis Melbourne Hotel and Apartments | 5 – 21 Therry Street, 3000 Melbourne, Australia

Local organising committee

This conference has been organised by the Australian Functional Genomics Network and driven by the committee members listed below.

The AFGN is a national consortium with the principal aim of fostering collaboration between model organism researchers, human geneticists, and clinicians. The AFGN works by harnessing the resource of model systems to determine the potential pathogenicity of disease-linked rare variants, gain a deeper pathophysiological understanding of diseases, and discover potential therapies for patients and families. Therefore enabling a ‘clinic to bench and back’ integrative approach of diagnostic services, incorporating laboratory research and clinical delivery for the efficient understanding of potentially pathogenic gene variants.

Prof Andrew Sinclair (Co-chair)

Murdoch Children's Research Institute

Prof Robert Bryson-Richardson

Monash University

Assoc Prof Kelly Smith

The University of Melbourne

Prof Gary Hime

The University of Melbourne

Prof Seth Masters

Walter and Eliza Hall Institute

Dr Tessa Mattiske

Murdoch Children’s Research Institute

Ebony Matotek

Murdoch Children's Research Institute