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DTSTAMP:20260624T161846Z
UID:530d475f-89c7-405b-9f7d-c1b27520ca7b
DTSTART:20260130T090000Z
DTEND:20260130T170000Z
DESCRIPTION:Understanding genomic variation is essential for uncovering the
  genetic basis of disease\, evolution\, and phenotypic traits. While short
 -read sequencing has long been the standard\, long-read technologies now o
 ffer superior resolution for detecting structural variants and phasing com
 plex regions. This course is designed for researchers working with genomi
 c data who want to explore the potential of long-read sequencing in varian
 t analysis. Participants will gain hands-on experience using the GenomeCom
 b package (https://derijkp.github.io/genomecomb/) to process long-read (an
 d short-read) data\, perform variant and structural variant calling\, and 
 annotate results. By the end of the training\, attendees will be equipped
  to apply these methods to their own datasets and interpret the biological
  relevance of the findings.
LOCATION:Ghent - VIB/UGent FSVM II\, Technologiepark 75
SUMMARY:Variant analysis using long-reads
URL;VALUE=URI:https://training.vib.be/all-trainings/variant-analysis-using-
 long-reads
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