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BioDiscovery - Gene Panels
The MSR algorithm can be applied to any gene panel from single gene (e.g. DMD test) to large panels having thousands of gene. The image below is from the Illumina TruSightTM Oncology 500 (TSO500) panel showing a somatic cancer profile. The cytogenetic complexity of the tumor sample is clearly evident with a large copy number gain of 8p and loss of a large section of 13q. Aberrations associated with genomic scarring, such as Loss of Heterozygosity (LOH), telomeric allelic imbalances (TAI), and large-scale state transitions (LST) can be visualized and manually called with confidence.
Detect, display, and decide-all from one place.
Detect.
You can’t diagnose what you can’t see. NxClinical is the gold standard for calling CNVs from NGS data generated on any platform.
Display.
Context is everything! NxClinical provides integrated analysis and raw data visualization of CNV, SNV, and AOH simultaneously on the same screen for each patient sample.
Decide.
Make the right call in record time. AI-driven tools and extensive automation enable rapid and accurate interpretation. Active links to the latest databases keep your knowledge base fresh and up-to-date.