Welcome to Cancer Genomics¶
The University of Sydney¶
25th - 27th July 2017¶
The Cancer Genomics workshop aims to provide an introduction to cancer genomics analytical pipelines for single nucleotide variations (SNV), copy number variations (CNV) and structural variations (SV).
Workshop Content¶
By the end of the course participants will be able to:
• Ability to perform NGS alignment and manipulate the output,
• Consider and plan experimental design,
• Be able to identify and generate variants (SNV, CNV, SV, Indels),
• Interpret variants with potential clinical interest,
• Be able to visualise and present data
This workshop will be delivered using a mixture of lectures, hands-on practical sessions, and open discussions.
Acknowledgements¶
This workshop was developed by Bioplatforms Australia, in partnership with CSIRO, and with support from the European Bioinformatics Institute (EBI), a member of the European Molecular Biology Laboratory (EMBL) in the UK. The workshop content has been maintained and updated by a network of dedicated [bioinformatics trainers] (http://www.bioplatforms.com/bioinformatics-training/) from around Australia.
The Bioinformatics Training Platform was developed in collaboration with the Monash Bioinformatics Platform and this workshop has been hosted on Interset infrastructure.
This workshop is possible thanks to funding support from the NSW Office of Health and Medical Research and the Commonwealth Government National Collaborative Research Infrastructure Strategy (NCRIS).