This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
It is estimated that 15–20% of clinically recognized pregnancies end in miscarriage and at least 50% of these losses result from a chromosomal abnormality.
NxClinical 3.0, a truly integrated system for analysis, visualization, and interpretation of data generated by both microarray as well as NGS platforms.
NxClinical uses VIA, applying a decision tree machine learning approach for automatic pre-classification of events to be interpreted by lab personnel.
NxClinical 2.1 is a revolutionary tool single integrated platform-independent solution that manages the entire data processing experience. Learn more.