- Qualitative analysis designed to identify point variants and small insertions/deletions in coding and non-coding exons, splice sites, and, partially, in the UTR regions of the BRCA1 and BRCA2 genes.
- Cannot detect large deletions and/or insertions.
- Bioinformatic analysis with the Datagenomics software.
- Amplicon-based NGS protocol.
- STIDs can be included: Integrated sample identification and tracking system
- Germline testing:
- Coverage: 100% of bases covered at DP100.
- Uniformity: 100% of bases covered at >20% mean coverage.
- Somatic testing: Limit of detection 5%
- Coverage: 99.8% of bases covered at DP1000.
- Uniformity: 99.8% of bases covered at >20% mean coverage.
- Sensitivity and specificity >99%.
- Repeatability and reproducibility >99%.
- For in vitro diagnostic use.
Through ClientSite you can filter variants and download your reports