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DTSTAMP:20260818T115753Z
UID:3bd4c125-4c52-458d-9e95-6ee834ed8956
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. 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.  You have the opportunity to explore the tools using your own da
 ta. Questions that arise during this process (about the tools\, the parame
 ters\, or the interpretation of the results) will be answered during the Q
 &amp\;A session. 
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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