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VERSION:2.0
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CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260710T142252Z
UID:567cabe4-86e4-4d7b-aa27-3a7900fe8e8d
DTSTART:20170504T233000Z
DTEND:20170505T023000Z
DESCRIPTION:In this tutorial we cover the concepts of detecting small varia
 nts (SNVs and indels) in human genomic DNA using a small set of reads from
  chromosome 22. The tutorial is designed to introduce the tools\, datatype
 s and workflow of variant detection. We will align reads to the genome\, l
 ook for differences between reads and reference genome sequence\, and filt
 er the detected genomic variation manually to understand the computational
  basis of variant calling.\n\n
LOCATION:Melbourne Bioinformatics\, Lab-14\, 700 Swanston Street
SUMMARY:Variant Calling with Galaxy and the GVL for beginners
URL;VALUE=URI:https://www.melbournebioinformatics.org.au/training-and-event
 s/
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