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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260813T192853Z
UID:9dd3b170-91ae-461b-83ed-66f846edca8d
DTSTART:20160527T090000Z
DTEND:20160527T000000Z
DESCRIPTION:Variant Detection using Galaxy is a one-day\, hands-on workshop
  that will cover the concepts of detecting small variants\, including SNPs
  and small indels\, from next-generation sequencing data. You will use and
  compare a number of popular detection tools\, visualise variants using a 
 genome browser\, and annotate SNPs for predicting biological effects.\nCou
 rse Outline\n-During this course you will learn about\;\n-The tool and wor
 kflows of SNP and indel detection\n-Quality filtering and other techniques
  for improving SNP prediction accuracy\n-Comparison of variant detection s
 oftware\n-the use of the Galaxy platform for variant detection analysis
LOCATION:Children’s Medical Research Institute
SUMMARY:Variant Detection Using Galaxy 
URL;VALUE=URI:http://www.bioplatforms.com/variant-detection-using-galaxy-ma
 y-2016/
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