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
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)
