Accel-Amplicon HS EGFR Panel
- Detect SNVs & indels down to 0.25%
- Requires only 10-50 ng cfDNA
- 3-hour Illumina-compatible library prep
- Covers EGFR, BRAF, KRAS & NRAS hotspots
Confident Detection of Low Frequency Variants
The new Amplicon HS EGFR Panel enables ultra-low frequency variant detection at 0.25-1% MAF from 10-50 ng of cell-free DNA (cfDNA) on Illumina® sequencers.
Nucleotide errors, normally introduced during PCR and sequencing, are removed through the use of unique molecular identifiers (MIDs or UMIs) that uniquely label target templates during amplification.
Components provided: target specific primer pool + PCR and library preparation reagents including indexing primers.