In this 30-minute webinar, presented by Sam Dougaparsad, learn how N_xClinical seamlessly uncovers compound heterozygous aberrations from any array or NGS platform.

Combining molecular data from array and sequencing has helped clinicians to better investigate the Human Genome for Recessive Disorders and Molecular Oncology.

While promised improvements in clinical diagnosis and utilities have been reported with NGS, how do we streamline the analysis of 1,000s of events (Copy Number, Allelic Imbalance and Sequence Variants) and their combinatorial effects, into a simple workflow?

When looking for focal aberrations, finding the needle in a haystack does not need to be time-consuming.