BEGIN:VCALENDAR
VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260808T233151Z
UID:92bbf42d-eb95-48f8-9512-28478a690b8b
DTSTART:20230418T083000Z
DTEND:20230421T163000Z
DESCRIPTION:This workshop will focus on the core steps involved in calling 
 variants from Illumina next generation sequencing data using the Genome An
 alysis Toolkit (GATK). You will learn about best practices in calling soma
 tic variants: single nucleotide variants (SNVs)\, short insertion/deletion
 s (indels) and copy number variants (CNVs). We will also cover considerati
 ons to take when calling variants on the mitochondrial genome\, as well as
  variant calling from bulk and single-cell RNA-seq data. We will also cove
 r how the data structures provided by GATK can help you process large data
 sets in parallel and at scale. \nAlthough this workshop focuses on human d
 ata\, the majority of the concepts and approaches apply to non-human data\
 , and we will cover some adaptations needed in those situations. \n\nThe t
 raining room is located on the first floor and there is currently no wheel
 chair or level access available to this level.\n\nPlease note that if you 
 are not eligible for a University of Cambridge [Raven](http://www.ucs.cam.
 ac.uk/docs/faq/raven/n5) account you will need to Book or register Interes
 t by linking [here](http://bioinfotraining.bio.cam.ac.uk/booking-form/?eve
 nt-id=4616411&amp\;course-title=Variant%20Discovery%20with%20GATK4).''
LOCATION:Craik-Marshall Building
SUMMARY:Variant Discovery with GATK4 (IN PERSON)
URL;VALUE=URI:http://training.csx.cam.ac.uk/bioinformatics/event/4616411
END:VEVENT
END:VCALENDAR