This conference has been organised by the Australian Functional Genomics Network due to the increasing clinical need for functional genomics in the patient diagnostic pipeline.

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 rapid translation of genomic findings into a patient diagnosis.

Register

Rare Disease: Australian Functional Genomics Conference

Fri 14 Sep 2018 8:30amSat 15 Sep 2018 7:30am

Venue

Unit 400/30 Flemington Road
Parkville VIC 3052
Room: 
Bio21 Institute

This conference with highlight:

  • The power of well-designed biological modelling for clinical gene variant interpretation.
  • Disease modelling for therapeutic design
  • Need for high-throughput mutational screening
  • The importance of the bi-directional exchange of ideas and information between clinical medicine and biomedical research