Hereditary Disease Solution (HDS)
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CatalogOncologySolid Tumor
The STS and STS Plus Solid Tumor NGS solutions are designed for the analysis of 42 relevant genes associated with the development of the most common solid tumors: lung, colorectal, skin and brain cancer, from DNA extracted from FFPE, fresh or frozen tissue. It also covers 6 unique loci to detect MSI status associated with colorectal cancer.
Both solutions allow accurate detection of SNVs, Indels and CNVs (in 24 genes), and Microsatellite Instability (MSI) status. The STS Plus solution also targets 137 fusion genes.
STS and STS Plus offer a streamlined sample-to-report workflow, which makes variant assessment quicker and easier, ensuring reliable results.
These NGS solutions include a capture-based target enrichment kit, as well as the functionality and analytical capabilities of the SOPHiA DDM™ platform for data interpretation. Sequencing can be performed on Illumina platforms.
The SOPHiA DDM™ platform features intuitive variant filters and prioritization options to streamline the interpretation process.
In addition to the STS and STS Plus solutions, other solutions are available for clinical diagnostics in areas such as metabolism, oncology, genetics or cardiology.
Available formats |
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16 test |
32 test |
48 test |
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