BEGIN:VCALENDAR
VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260620T093006Z
UID:8864e64a-2804-4144-9933-20fa5d2c14b1
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/
END:VEVENT
END:VCALENDAR