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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260711T125029Z
UID:8f0f20f7-f283-4d53-a91b-4144ff213c50
DTSTART:20190530T093000Z
DTEND:20190531T170000Z
DESCRIPTION:This course covers state-of-the-art and best-practice tools for
  the analysis of genomes. We describe\, and give hands-on experience of\, 
 the entire analysis workflow from raw data generated by a sequencing machi
 ne to deriving variant calls (e.g. Single Nucleotide Variants) that are re
 ady for downstream analysis\, interpretation and prioritisation. We will d
 escribe the steps involved to go from sequencing library to a prioritised\
 , clinically-relevant list of DNA variants. Practical sessions will use th
 e user-friendly Galaxy interface (https://usegalaxy.org/) to demonstrate t
 asks such as alignment\, quality control\, variant-calling and annotation.
LOCATION:The Diamond\, Workroom 1
SUMMARY:Introduction to Genomic Variant Interpretation
URL;VALUE=URI:http://sbc.shef.ac.uk/training/variants-introduction-2019-05-
 30
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