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DTSTAMP:20260721T092305Z
UID:cc3b5e8a-a8d1-4f0a-9ece-e71fcefded3a
DTSTART:20200120T090000Z
DTEND:20200121T000000Z
DESCRIPTION:Using a full publicly available chromosome read-set from one of
  the 1000 genome samples:\n\n\n	​Perform a complete analysis workflow in
 cluding QC\, read mapping\, read coverage analysis\, and variant calling a
 gainst the human reference genome.\n	Use GenePattern and open source softw
 are to evaluate each step of a classical NGS variant workflow and feel the
  complexity of the task.\n	Quickly compare the obtained results with gold 
 standard public data\n\n\nThe skills acquired during this session should a
 llow participants understand what variant calling implies. \n\nParticipant
 s with experience in command line can do the workflow using command line t
 ools.
LOCATION:iGent
SUMMARY:Hands-On introduction to NGS variant analysis
URL;VALUE=URI:https://training.vib.be/product/149
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