truNGS® Endometrial Cancer Panel Kit

This product is designed to detect SNVs, Indels and CNVs in 31 marker genes and hotspots in 6 pharmacogenomics genes associated with endometrial cancer from nucleic acid extracted from fresh frozen/formalin fixed paraffin embedded (FFPE) tissue.

The kit has been designed to detect SNVs, Indels and CNVs in DNA isolated from formalin-fixed, paraffin embedded (FFPE) tumor tissue specimens. The protocol involves two major steps:

(A) Library preparation (input DNA fragmentation, adapters ligation, PCR amplification of individual libraries); and

(B) Hybrid Capture and target enrichment (library pooling, probes hybridization, capture, and post- capture PCR amplification)

For use on Illumina and MGI platforms only