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DTSTAMP:20260806T132716Z
UID:acb427a1-e8a8-4253-a77f-536bf087b50e
DTSTART:20270127T090000Z
DTEND:20270127T170000Z
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. You will gain hands-on experience using the GenomeComb package
  (https://derijkp.github.io/genomecomb/) to process long-read (and short-r
 ead) data\, perform variant and structural variant calling\, and annotate 
 results. 
LOCATION:Antwerp - Campus Drie Eiken UAntwerpen\, Universiteitsplein 1
SUMMARY:Variant analysis using long-reads
URL;VALUE=URI:https://training.vib.be/all-trainings/variant-analysis-using-
 long-reads-0
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