Dear all, I am happy to announce that for the third year in a row we have been able to get three members of the GATK team of the Broad Institute ( https://software.broadinstitute.org/gatk/) over to Edinburgh for a few days to teach a workshop on GATK Best Practices for Variant Discovery. Details of the workshop can be found below. With kind regards, Bert ********** GATK BEST PRACTICES FOR VARIANT DISCOVERY DATE: Monday 17 - Wednesday 19 July 2017 VENUE: The King's Buildings,The University of Edinburgh, Edinburgh, Scotland, UK REGISTRATION DEADLINE: Monday 3 July 2017 CANCELLATION DEADLINE: Monday 10 July 2017 PLACES: 85 (lectures), 30 (hands-on sessions) (first come, first served) REGISTRATION FEE: £70 for the lectures, £35 for each half-day hands-on session (includes coffee/tea, but no lunch) INFORMATION: Bert Overduin (bert.overduin@ed.ac.uk) TO REGISTER: http://genomics.ed.ac.uk/services/gatk-best-practices-variant-discovery This workshop will focus 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. In the course of this workshop, we highlight key functionalities such as the GVCF workflow for joint variant discovery in cohorts, RNAseq-specific processing, and somatic variant discovery using MuTect2. We also preview capabilities of the upcoming GATK version 4, including a new workflow for CNV discovery, and we demonstrate the use of pipelining tools to assemble and execute GATK workflows. "Excellent opportunity to learn from world-renowned experts!" (April 2016) INSTRUCTORS GATK staff (The Broad Institute, Cambridge, MA, United States) WORKSHOP FORMAT The workshop is composed of one day of lectures (including many opportunities for Q&A) and two optional days of hands-on training, structured as follows: Lectures (day 1): Rationale, theory and application of the GATK Best Practices for Variant Discovery in high-throughput sequencing data. Hands-on 1 (day 2 am): Germline variant discovery (SNPs + Indels) Hands-on 2 (day 2 pm): Germline variant filtering (SNPs + Indels) Hands-on 3 (day 3 am): Somatic variant discovery (SNPs + Indels + CNV) Hands-on 4 (day 3 pm): Pipelining on the cloud with WDL Please note that the lectures part is mandatory. It is not possible to attend any of the hands-on sessions without attending the lectures. In the three optional hands-on sessions focused on analysis, we walk attendees through exercises that teach them how to manipulate the standard data formats involved in variant discovery and how to apply GATK tools appropriately to common use cases and data types. In the course of these exercises, we demonstrate useful tips and tricks for interacting with GATK and Picard tools, dealing with problems, and using third-party tools such as Samtools, IGV, RStudio and RTG Tools. In the optional hands-on session on pipelining, we walk attendees through exercises that teach them to write workflow scripts using WDL, the Broad's new Workflow Description Language, and to execute these workflows locally as well as through publicly available cloud-based services. Please note that this workshop is focused on human data analysis. The majority of the materials presented applies equally to non-human data, and we will address some questions regarding adaptations that are needed for analysis of non-human data, but we will not go into much detail on those points. WHO SHOULD ATTEND The lecture-based component of the workshop is aimed at a mixed audience of people who are new to the topic of variant discovery or to GATK, seeking an introductory course into the tools, or who are already GATK users seeking to improve their understanding of and proficiency with the tools. Attendees should already be familiar with the basic terms and concepts of genetics and genomics. The hands-on component is aimed at novice to intermediate users who are seeking detailed guidance with GATK and related tools. Basic familiarity with the command line environment is required. Please note that for the hands-on sessions attendees will be expected to bring their own laptops with software preinstalled (detailed instructions will be posted two weeks before the workshop). Supported systems are Mac and Unix/Linux systems. MS Windows is not supported. COVERED TOPICS Lectures Introduction to variant discovery analysis and GATK Best Practices Marking Duplicates Indel Realignment Base Recalibration Variant Calling and Joint Genotyping Filtering variants with VQSR Genotype Refinement Workflow Callset Evaluation Somatic variant discovery with MuTect2 Preview of CNV discovery with GATK4 Hands-on 1 Germline variant discovery (SNPs + Indels) Hands-on 2 Germline variant filtering (SNPs + Indels) Hands-on 3 Somatic variant discovery (SNPs + Indels + CNV) Hands-on 4 Pipelining on the cloud with WDL -- Bert Overduin, PhD TRAINING AND OUTREACH BIOINFORMATICIAN Bert.Overduin@ed.ac.uk orcid.org/0000-0002-5281-8838 EDINBURGH GENOMICS The University of Edinburgh Ashworth Laboratories The King's Buildings Charlotte Auerbach Road Edinburgh EH9 3FL Scotland, United Kingdom tel. +44(0)1316507403 http://genomics.ed.ac.uk The University of Edinburgh is a charitable body, registered in Scotland, with registration number SC005336.