- Dynamic kit that updates the target genes of the panel according to scientific evidence.
- Type of mutations analyzed: SNVs, INDELs, CNVs, ALUs and other large insertions.
- Coverage: 99.5% of bases covered at a depth of 50X.
- Uniformity: 99.2% of the bases covered at >20% of the average coverage and 90.0% of the bases covered at >50% of the average coverage.
- Sensitivity: > 99.9%
- Specificity: > 99.9%
- Necessary reagents to perform libraries indexing reactions are not included
- For in vitro diagnostic use.
Through ClientSite you can filter variants and download your reports