BEGIN:VCALENDAR
VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260617T130304Z
UID:478e6203-ca0e-4248-9ea2-a538e4be1333
DTSTART:20211129T130000Z
DTEND:20211206T170000Z
DESCRIPTION:This course covers state-of-the-art and best-practice tools for
  the analysis of genomes and transcriptomes. We describe\, and give hands-
 on experience of\, the entire analysis workflow from raw data generated by
  a sequencing machine to deriving variant calls (e.g. Single Nucleotide Va
 riants) that are ready for downstream analysis\, interpretation and priori
 tisation. We will describe the steps involved to go from sequencing librar
 y to a prioritised\, clinically-relevant list of DNA variants. Practical s
 essions will use the user-friendly Galaxy interface (https://usegalaxy.org
 /) to demonstrate tasks such as alignment\, quality control\, variant-call
 ing and annotation.
LOCATION:ONLINE
SUMMARY:Intro to Next Generation Sequencing and Bioinformatics
URL;VALUE=URI:http://sbc.shef.ac.uk/training/ngs-introduction-2021-11
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