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DTSTAMP:20260627T214049Z
UID:a4cb9fd3-9ce6-47bf-8c4f-c56a167778ed
DTSTART:20240516T150000Z
DTEND:20240516T150000Z
DESCRIPTION:Abstract:\n\n				Genomic copy number variants (CNV) are a major
  contributor to human genome variation and important factors in rare disea
 se genetics and cancer genomics. However\, the complexity of CNV detection
  technologies\, the lack of standardised annotation formats and the fragme
 ntation of cytogenetic and genomic communities so far has limited large sc
 ale utilization of CNV profiles in computational genomics. Here\, the ELIX
 IR hCNV community provides a group of experts with various (cyto-)genetic\
 , genomic and computational backgrounds\, working on common standards\, im
 plementations\, workflows\, training and documentation relevant for struct
 ural genome variation analysis\, utilization and data sharing aspects.\n		
 	\n			 \n		\n	\n\n\n\n	\n		\n			\n				Speakers\n\n				\n					\n						\n		
 					\n							\n							\n						\n						\n							\n								Dr Michael Baudi
 s\n\n								The University of Zurich\n							\n							\n								Dr Antoni
 o Rausell  \n\n								Imagine Institute of Genetic Diseases\n							\n	
 						\n								  Dr Krzysztof\n\n								  Poterlowicz \n\n								 
  The University of Bradford\n							\n						\n						\n							\n								 \
 n							\n						\n					\n				\n\n				Talks: \n\n				    1. Implementati
 on driven development of CNV representation\n\n				        standards
  and variant discovery protocols\n\n				    2. hCNV Galaxy ecosystem 
  \n			\n		\n		\n			 
SUMMARY:The ELIXIR hCNV Community - Making complex genomics accessible
URL;VALUE=URI:https://www.elixir-europe.org/events/elixir-hcnv-community-ma
 king-complex-genomics-accessible
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