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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260818T082406Z
UID:f7cbb1b4-8ed2-41ce-949a-70e4587e2f74
DTSTART:20190510T093000Z
DTEND:20190510T170000Z
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:Pam Liversidge Design Studio 1 - D06
SUMMARY:Introduction to identifying and characterising somatic variants
URL;VALUE=URI:http://sbc.shef.ac.uk/training/somatic-variants-introduction-
 2019-05-10
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