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VERSION:2.0
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BEGIN:VEVENT
DTSTAMP:20260616T231444Z
UID:cd44ef93-efd2-49d2-817a-83a1924926f7
DTSTART:20260521T090000Z
DTEND:20260521T170000Z
DESCRIPTION:Genomic structural variants (large-scale rearrangements in DNA)
  are increasingly recognised as drivers of disease risk and genome diversi
 ty\, yet they are difficult to explore between genome assemblies. The new 
 Alignments viewer on the Ensembl Data Platform allows you to easily browse
  alignments and structural variants. In this webinar\, we will explain ho
 w genomic alignments are generated and how structural variants are identif
 ied and imported into Ensembl. We will demonstrate the Alignments viewer l
 ive\, showing you how to compare human reference and alternative assemblie
 s.
LOCATION:\, 
SUMMARY:The new Ensembl Alignments viewer tool for exploring genomic struct
 ural variation
URL;VALUE=URI:https://www.ebi.ac.uk/training/events/new-ensembl-alignments-
 viewer-tool-exploring-genomic-structural-variation
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