We’re moving the GATK website, docs and forum to a new platform. Read the full story and breakdown of key changes on this blog.
If you happen to see a question you know the answer to, please do chime in and help your fellow community members. We encourage our fourm members to be more involved, jump in and help out your fellow researchers with their questions. GATK forum is a community forum and helping each other with using GATK tools and research is the cornerstone of our success as a genomics research community.We appreciate your help!
Test-drive the GATK tools and Best Practices pipelines on Terra
Check out this blog post to learn how you can get started with GATK and try out the pipelines in preconfigured workspaces (with a user-friendly interface!) without having to install anything.
Away Workshop (Brussels) 2014 June 24-26: Best Practices for Variant Calling with GATK
Laura Gauthier, David Roazen and Geraldine Van der Auwera presented this workshop in Brussels, Belgium, upon invitation from the Royal Belgian Institute for Natural Sciences.
This workshop included two modules:
Best Practices for Variant Calling with the GATK
The core steps involved in calling variants with the Broad’s Genome Analysis Toolkit, using the “Best Practices” developed by the GATK team. The presentation materials describe why each step is essential to the calling process, what are the key 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.
Beyond the Best Practices
Additional considerations such as calling variants in RNAseq data and calling cohorts efficiently, as well as dealing with non-human data, RNAseq data, whole-genome vs. exome, basic quality control, and performance.
This was complemented by a set of hands-on exercises aiming to teach basic GATK usage to new users.
The workshop materials are available at this link if you're viewing this post in the forum, or below if you are viewing the presentation page already.