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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
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DTSTAMP:20260716T204547Z
UID:6701017c-8b9b-4290-9d1a-fc6e6826ecec
DTSTART:20200421T093000Z
DTEND:20200521T170000Z
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 identifying and characterising somatic variants
URL;VALUE=URI:http://sbc.shef.ac.uk/training/somatic-variants-introduction-
 2020-04-21
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