From: Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine
Known
Detected
Sensitivity
BRAF V600E
1
1.00
CTNNB1 D32G
EGFR micro deletion
7
6 (7)
0.86 (1)a
EGFR SNV
14
13 (14)
0.93 (1)
KRAS SNV
MET SNV
NRAS SNV
3