TruNGS® Solid Tumor Panel Kit (Inclusief Bioinformatic workflow en rapportage)

• RUO (Research Use Only) • Carefully curated panel of 35 genes with Clinical Actionability (mutations especially relevant to lung and colorectal cancers • Designed as per NCCN and ESMO Guidelines • Detects SNV/INDELS, CNV and RNA Fusions • Uses Hybrid Capture technology to ensure full coverage of all exonic regions of each gene and allows for the discovery of novel mutations/alterations • Includes hotspot for six clinically relevant pharmacogenomics genes DPYD, UGT 1 A 1, CYP 2 D 6 MTHFR, TPMT and CYP 2 C 9 • LoD as low as 3 5 % (calculated for SNV using reference material at 500 X)

The Solid Tumor Panel is designed to detect SNVs, Indels CNVs and RNA fusions in 35 marker genes and hotspots in 6 pharmocogenomics genes associated with solid tumors such as lung, gastro intestinal/colorectal, breast, liver and ovarian tumors. For use on Illumina and MGI platforms only. The Solid Tumor flyer can be found here An example of the report can be found here