Time: 9:00:00 am
Address: Australian National University|Canberra|ACT|-|AU
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).
Topics that will be covered during this workshop include: experimental design, variant calling, annotation and visualisation of cancer genome data.
By the end of the course participants will be able to perform NGS alignment and manipulate the output, consider and plan experimental design, identify and generate variants (SNV, CNV, SV, Indels), interpret variants with potential clinical interest, visualise and present data.