The Rare Disease: Australian Functional Genomics National Conference will bring together the diverse model systems communities involved in disease gene discovery and characterisation, with the aim of enabling the rapid translation of genomics findings to a diagnosis of disease.
Invited speakers will showcase the increasing need for functional genomics in the patient diagnosis pipeline and the benefits and logistics of an array of model organism research for variant classification and therapeutic screening.
Abstract Submission open now and close August 13th
Check here for the more information, the program, registration and abstraction submission.
Prof. Phil Beales, UCL Great Ormond Street Institute of Child Health
Diagnosis of rare genetic disorders and understanding the molecular basis of disease.
Prof. Steve Brown, MRC Harwell Institute
Deciphering the genetic bases of disease: the role of the mouse
Featured National Speakers:
Prof. Kathryn North, Prof. Andrew Sinclair, Prof. Ian Alexander, Prof. Kieran Harvey, A/Prof. Ben Hogan, Dr. Mark Corbett, A/Prof. Shane Grey, Prof. Steve Petrou, Prof. Richard Harvey, Prof. Sally Dunwoodie, Dr Alan Rubin, A/Prof. Alice Pebay, Prof. Sandra Cooper, A/Prof. Bruce Bennetts, Dr Emma Palmer, Dr Zornitza Stark
Venue: Bio 21 Auditorium
Address: Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Unit 400/30 Flemington Rd, Parkville VIC 3052
Date/Time: 10 am Friday September 14th – 1:30 pm Saturday September 15th
Social Function: 6:30-9:30 pm Friday September 14th @ Melbourne Museum
(included in your conference registration ticket)