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DTSTAMP:20260707T041703Z
UID:ac7c482d-415b-4643-ab8e-96442343d506
DTSTART:20160608T090000Z
DTEND:20160608T000000Z
DESCRIPTION:This tutorial covers the concepts of detecting small variants (
 SNVs and indels) in human genomic DNA using a small set of reads from chro
 mosome 22. The tutorial is designed to introduce the tools\, datatypes and
  workflow of variant detection. We will align reads to the genome\, look f
 or differences between reads and reference genome sequence\, and filter th
 e detected genomic variation manually to understand the computational basi
 s of variant calling.\n
LOCATION:Lab-14\, VLSCI
SUMMARY:Variant Calling with Galaxy and the Genomics Virtual Laboratory (be
 ginners)
URL;VALUE=URI:https://variant-calling-galaxy-beginners.eventbrite.com.au
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