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CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260808T165408Z
UID:6d443939-04e1-4b25-aaaa-56d6700b8717
DTSTART:20181109T093000Z
DTEND:20181116T170000Z
DESCRIPTION:b'Using a full publicly available chromosome read-set from one 
 of the 1000 genome sample:\\r\n\\r\n\n This training gives an introduction
  to the use of several\\r\npopular NGS analysis software packages under th
 e GenePattern Graphical\\r\ninterface.\\r\n\n Skills required to follow th
 is training include basic knowledge of Illumina NGS read structure. People
  who lack knowledge of Illumina reads should follow the \\'Introduction t
 o the analysis of NGS data\\' training. Depending on the number of parti
 cipants (max 20)\, it might be that you have to share the laptop with one 
 other participant but you can also choose to bring your own laptop for th
 is training session.​\n\\r\n\n \n\nsimilar workflow(s) using unix operat
 ive system and the command-line\\r\napproach.​\\r\n​similar workflow(s
 ) using commercial products like the \\'CLC genomics workbench\\'\\r\nsimi
 lar workflow(s) using the free Galaxy GUI (although perfectly doable using
  the acquired knowledge)\\r\nvariant analysis at multi-genome level &amp\;
  GWAS (&lt\;- advanced computing and statistical expertise required).\\r\n
 structural variant analysis (large indels\, translocations\, CNV) as being
  too complex with no all-in-one tool available.\n\\r\n\\r\n​​​​​
 ​​​​​​​​​​​​\n'
LOCATION:Park Inn by Radisson Leuven
SUMMARY:Hands-On introduction to NGS variant analysis
URL;VALUE=URI:http://www.vib.be/en/training/research-training/courses/Pages
 /Hands-On-introduction-to-NGS-variant-analysis.aspx
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