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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260707T093024Z
UID:c8fdfa03-ad5c-4726-ac9d-325eb8e443ba
DTSTART:20171204T090000Z
DTEND:20171205T170000Z
DESCRIPTION:This course is aimed at clinicians and wet-lab biologists who a
 re involved in research projects requiring the analysis of exome data\, in
 terpretation of sequence variation identified during genomic analyses\, an
 d preparing accurate sequence variation descriptions for publication\, cli
 nical reporting and data basing. Attendees will receive an introduction to
  calling variants and copy number alterations from exome sequencing data a
 lignment files\, reference sequences\, variation nomenclature\, variant an
 notation\, variant effect prediction\, and clinical and publication report
 ing recommendations.\n\nThis course serves as the second in a two-part wor
 kshop. The first part\, an Introduction to DNA-seq\, will be held in Novem
 ber 2017. While attendance of the November workshop is not a pre-requisite
 \, familiarity with the topics it covers will be necessary.
LOCATION:College Court
SUMMARY:Exome Variants\, Copy Number Calling\, Variant Annotation and Repor
 ting workshop\, December 2017 
URL;VALUE=URI:https://www2.le.ac.uk/colleges/medbiopsych/facilities-and-ser
 vices/cbs/bbash/training/workshop-webpages/dna-seq-ngs-dec2017
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