- NGS panel for the study of the main clinically relevant biomarkers for the most common solid tumors in adults.
- It allows detecting SNVs, indels, genetic fusions, CNVs, pharmacogenetic variants, and microsatellite instability analysis (MSI) from a single DNA sample.
- Bioinformatics analysis with the Datagenomics software and semiautomated generation of reports, including functional and clinical classification of the identified variants.
- STIDs can be included: Integrated sample identification and tracking system.
- Based on high sensitivity RNA-probe technology with UMI barcoding (unique molecular identifiers).
- Mean coverage: 2500X and mean coverage after UMI analysis: 1600X.
- Coverage (at depth >100x), specificity, sensitivity, repeatability, and reproducibility of this test are over 99%. The uniformity of bases covered at >20x is 98.8%.
- Technical support starting with the implementation of the first protocol, available both online and on-site. All protocols will be set up in collaboration with your laboratory personnel.
- STID: Clinical support and genetic counseling. Our team of specialists can help you with any query you may have regarding cancer genetics.
- Possibility of sending 10% of your samples to our laboratory at no additional cost during periods of excessive laboratory workload or urgent deadlines.
- Possibility of handling your projects as service at Health in Code laboratories (TAT: 10 working days).
Through ClientSite you can filter variants and download your reports