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 2.1 is a revolutionary tool single integrated platform-independent solution that manages the entire data processing experience. Learn more.
Bert Eussen gives some helpful hints for those studying copy number variation from arrays or NGS and need an alternate method for validation of CNVs.
In this webinar, we will examine a few different cases of early-onset epilepsy and hyperphosphatasia with intellectual disability, better known as Mabry syndrome, an autosomal recessive form of ID.
Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.