- 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).
- It complies with the quality requirements specified by ISO 13485 and ISO 14001 in relation to the materials used in its manufacturing process.
Through ClientSite you can filter variants and download your reports
