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CentoWebinar on demand
CentoWebinar on demand - Solving the diagnostic riddle: Diagnosing heterogeneous genetic disorders with whole exome sequencing
Most of the disease-causing mutations that science has been able to identify so far are located within the exons. Whereas most genetic tests focus on a single gene or on a set number of predetermined genes, a whole exome sequencing test examines thousands of genes simultaneously.
CentoWebinar on demand - A race against the clock - Diagnosing genetic conditions in newborns and children
Up to one third of all babies and children admitted to the intensive care unit (ICU) have a genetic disease. For many of them early identification can make a difference for their immediate and later health.
CentoWebinar on demand - How whole genome sequencing is changing the status quo of medicine November 2016
WGS identifies nearly all changes in a patient’s DNA by sequencing the entire coding and non-coding regions of the genome and provides detailed information on the thousands of genes involved in normal growth and development and all of the ‘silent’ genome regions simultaneously.