This is a two-part virtual event with two different sessions in a European time zone (CEST) and North American time zone (EST).
An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.
10:00 – 10:30 am (CEST) | 1:00 – 1:30 pm (EST)
Simplify your secondary analysis from FASTQ to VCF in 5 steps
10:30 – 11:00 am (CEST) | 1:30 – 2:00 pm (EST)
Solve every hereditary disorder case for all types of genetic mutations
Why lab’s need high-quality, deeply curated knowledge to skip the diagnostic odyssey
How you can interpret complex germlines cases and increase your diagnostic yield with QCI Interpret
How QCI Interpret displays and interprets copy number variants
11:00 – 11:30 am (CEST) | 2:00 – 2:30 pm (EST)
Going beyond the exome
An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing.
Attendees will gain: