Table 1.
Gene Target | Idylla [7] | Ion PGM (NGS) [8] |
---|---|---|
EGFR | Idylla EGFR Mutation Test [9] Coverage: Exon 18 point mutations (G719A/C/S), exon 19 deletion (Del9, Del12, Del15, Del18, Del21, Del24), exon 20 point mutations (T790 M, S768I) and insertions (insG, insASV9, insASV11, insSVD, insH), exon 21 point mutations (L858R, L861Q) Detection limit: ‘≤ 5% for most prevalent EGFR mutations’ Turn-around time: 2 h (approx.) |
AmpliSeq Cancer Hotspot Panel v2 [6] Coverage†: Detection limit: 98% detection rate for 5% variant frequency at positions with average sequencing coverage from × 1000 to × 4000 Turn-around time: Single day |
*Terminating codon notation
†Coverage given is for the codon changes that are likely to be relevant in CRC