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A comprehensive NGS panel that, in addition to the detection of somatic mutations (SNV, InDel, CNV), also enables the determination of other relevant biomarkers such as microsatellite instability (MSI) and mutational burden (TMB).
Library preparation is based on hybridization capture technology.
Kits are validated for Illumina NGS sequencers.
The solution also includes the unique SOPHiA DDM software for secondary and tertiary analysis of the resulting NGS data.
For more information, please contact us by e-mail: diagnostika@pentagen.cz