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Panels for the detection of SNV, InDel and CNV somatic variants in 4-28 genes involved in the homologous recombination pathway. Library preparation is based on hybridization capture technology.
The kit is validated for Illumina NGS sequencers.
The solution also includes the unique SOPHiA DDM software for secondary and tertiary analysis of the resulting NGS data.
|
BS0111ILLRSMY05 |
SOPHiA DDM Mini Homologous Recombination Solution |
4 genes |
|
BS0108ILLRSMY05 |
SOPHiA DDM Homologous Recombination Solution |
16 genes |
|
BS0124ILLRSMY08 |
SOPHiA DDM Extended Homologous Recombination Solution |
28 genes |
For more information, please contact us by e-mail: diagnostika@pentagen.cz