truNGS® Solid Tumor Panel Kit

Solid Tumor Panel Kit

(Including Bioinformatics workflow and Reporting)

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.

Specifications

  • Starting Material: 50-100 ng of DNA, 300-600 ng RNA
  • Sample source: FFPE, Fresh Frozen Tissue
  • Target region for DNA Panel: 117 kb
  • Target region for RNA Panel: 74 kb
  • Library preparation time: 1.5 days
  • Bioinformatics Analysis: 1.5 hrs (from FASTQ to report)

Key Features:

  • 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)