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VERSION:2.0
PRODID:icalendar-ruby
CALSCALE:GREGORIAN
BEGIN:VEVENT
DTSTAMP:20260618T202243Z
UID:a3f1c293-b3de-4844-88fd-2a0bb6f6ed67
DTSTART:20171120T090000Z
DTEND:20171121T170000Z
DESCRIPTION:This two day course serves as the first in a larger two-part co
 urse in conjunction with our Exome Variants\, Copy Number Calling\, Varian
 t Annotation and Reporting workshop in December 2017\, as well as a standa
 lone introduction to DNA-seq. Attendees will receive an introduction to ne
 xt generation sequencing (NGS) platforms\, data analysis and tools for dat
 a quality control\, read alignment (mapping) and refinement using DNA-seq 
 data. The course will conclude with a basic introduction to variant callin
 g as a lead-in to the December workshop.
LOCATION:College Court
SUMMARY:Introduction to DNA-seq NGS Analysis Workshop\, November 2017 
URL;VALUE=URI:https://www2.le.ac.uk/colleges/medbiopsych/facilities-and-ser
 vices/cbs/bbash/training/workshop-webpages/dna-seq-ngs-nov2017
END:VEVENT
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