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A wide range of NGS kits for the detection of SNVs, InDels and CNVs in somatic and germinal samples.
The advantage of the kits is the use of molecular barcodes (MBCs) and an easy workflow thanks to a unique system of lyophilized reagents.
The Archer® Analysis v7 software with its own ArcherQuiver™ database connected to the Ensembl VEP, Clinvar and COSMIC databases is used to evaluate the results.
The preparation of the libraries is based on the unique patented AMP technology, the main advantages of which are robustness and easy customization of the panels.
DB0170 |
VariantPlex™ BRCA v2 |
2 genes |
DB0401 |
VariantPlex™ BRCA + PALB2 |
3 genes |
AB0077 |
VariantPlex™ CTL |
31 genes |
AB0139 |
VariantPlex™ Solid Tumor Focus v2 |
20 genes |
AB0140 |
VariantPlex™ Core Solid Tumor |
60 genes |
AB0076 |
VariantPlex™ Solid Tumor |
67 genes |
AB0141 |
VariantPlex™ Expanded Solid Tumor |
76 genes |
AB0142 |
VariantPlex™ Pan Solid Tumor |
185 genes |
AB0144 |
VariantPlex™ Complete Solid Tumor |
430 genes |
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VariantPlex™ Custom Panels |
Custom |
For more information, please contact us by e-mail: diagnostika@pentagen.cz