Jun 13, 2016 09:30 AM
Jun 14, 2016 05:30 PM
|Where||Bioinformatics Training Room, Craik-Marshall Building, Downing Site|
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This workshop focuses on the core steps involved in calling variants with the Broad’s Genome Analysis Toolkit, using the “Best Practices” developed by the GATK team. You will learn why each step is essential to the variant discovery process, what are the operations performed on the data at each step, and how to use the GATK tools to get the most accurate and reliable results out of your dataset.
The workshop is composed of one day of lectures (including many opportunities for Q&A) and one day of handson training.
For more information and to book, please visit.