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Next-Generation Sequencing
For library preparation with targeted NGS panels
For molecular tumor diagnostics and cancer research, we offer specialized panels for Next-Generation Sequencing (NGS) in collaboration with our partner AmoyDx®. The assays, which are compatible with Illumina sequencers, are based on two different library preparation methods: the straightforward HANDLE method, which is based on the use of modified molecular inversion probes, or the comprehensive ddCAP technology, a hybrid capture method. In all AmoyDx® NGS kits, UID (Unique IDentifier) sequences are used to correct PCR errors during data analysis. Sequence data analysis is performed locally using the AmoyDx® NGS Data Analysis System (ANDAS).
HANDLE Technology
ddCAP Technology
ANDAS
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