A 4-day course on NGS took place in Lisbon, Portugal in the period of 24-27 October 2016. The focus of the course was on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions. For more details and program of the course please click here.
"Alamut is the best tool I have used for the annotation of DNA variants. It has a great user interface, combines data from multiple sources and allows for ease of variant interpretation by clinical geneticists."
JORDAN LERNER-ELLIS, Ph.D.
Mt. Sinai Hospital, Toronto