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2008 Melbourne Information Seminar Presentations |
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- Richard Cotton - Welcome and Introduction (view | download)
- Myles Axton - Dealing with variant publication (view | download)
- John Hopper - Importance of accurate collection of data for inherited disease and common disease for research and treatment (view | download)
- Ingrid Winship - The Clinic - The ideal system (view | download)
- Agnes Bankier - Web based resources for the clinical geneticist (view | download)
- Desiree du Sart - The Diagnostic Lab - The ideal system (view | download)
- Les Sheffield - Introduction of National Pharmacogenomic testing - The ideal system (view | download)
- David Ravine - LSDB Curation - The ideal system (view | download)
- David Thorburn - Collection of data in Australia (view | download)
- Peter George - The Diagnostic Lab - what we've got and why we don't report it (view | download)
- Marienne Hibbert - BioGrid Australia - a virtual platform for multi-disease, multi-institutional research (formerly MMIM) (view | download)
- Ravi Savarirayan - The Human Variome: implications for musculoskeletal disease (view | download)
- Terence Harrison - Evidence Based Medicine system - Is genetics coverage sufficient? (view | download)
- Finlay Macrae - HNPCC as a model system - A HVP/InSiGHT pilot study (view | download)
- Lawrence Cavedon - The role of NICTA (view | download)
- Nicola Stokes - Text mining (view | download)
- Tim Smith - VariVis to depict variation (view | download)
- Bernard Brais - Collection of inherited neurological disease from a Quebec isolate (view | download)
- David Goldgar - Issues in Integration of multiple sources of evidence in clinical classification of sequence of variants of uncertain significance (view | download)
- Vijaya Sundararajan - NCRIS and its relevance to collecting variation and phenotypic data in the future (view | download)
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