NGS Targeted Enrichment Panel
The NGS panels are custom designed from end-to-end with your genes of interest. The pre-capture pooling and high panel performance enables cost and labour savings. Every designed panel is in-house validated on performance and functionality.
Targeted Sequencing selectively analysis specific regional sequences of genomes. By only analysing specifically, time and money are saved.
Via hybridisation based capture technology, the core process of targeted sequencing is enabled. Targeted Sequencing is the separation and analysis of specific regional sequences of the whole genome. Via targeted sequencing, all types of mutations can be accurately analyses: SNV, InDEL, CNV and Rearrangements.
The panels utilise an intrinsic probe design, rebalancing, and molecular barcode technologies. This ensures efficient analysis also hard-to-capture areas, such as GC-rich and homologous regions. Additionally, damaged DNA and RNA originated from circulating tumour cells or FFPE samples can easily be analysed.
