truNGS® Endometrial Cancer Panel Kit
(Including Bioinformatics workflow and Reporting)

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

RUO(Research Use Only)

The truNGS Endometrial Cancer Panel flyer can be found here

An example of the report can be found here