| 檢驗方法 |
次世代定序(Next-generation sequencing)
1. DNA Panel可偵測之基因：
ABL1, CTNNB1, MAP3K8, PTEN, BARD1, IRF1, PMS1, AKT1, DDR2, MET, RET, BRCA1, KIT, PMS2, ALK, EGFR, MYC, ROS1, BRCA2, MLH1, RAD51B, ATM, ERBB2, MYCN, SLC22A18, BRIP1, MLH3, RAD51C, BRAF, FGFR1, NRAS, STK11, CDK12, MSH2, RAD51D, CCND1, FGFR3, NTRK1, TP53, CHEK1, MSH3, RAD54L, CD274, HRAS, PIK3CA, TSC2, CHEK2, MSH6, RB1, CDK4, KRAS, PPP2R1B, BAP1, FANCL, PALB2, CDKN2A, MAP2K1, PRKN, NF2, IDH1, IDH2, PDGFRA。
2. RNA Panel可偵測之融合基因，包含驅動基因與診斷相關基因。
2.1驅動基因(Driver Gene)：
ALK, BRAF, RET, ROS1, RAF1, NTRK1, NTRK2, NTRK3, FGFR1, FGFR2, FGFR3, FGFR4, NRG1, EGFR, ERBB2, MET, KRAS
2.2診斷相關基因(Diagnosis relative gene)：
AR, AXL, BAIAP2L1, BCOR, CCDC6, CCNB3, CD74, CIC, CLTC, CREB3L2, CRTC1, EML4, ERG, ETV1, ETV6, EWSR1, EZR, FLI1, FOXO1, FUS, GOPC, HIP1, KIF5B, KLC1, KMTA2(MLL), LMNA, LRIG3, MAML2, MLLT10, MYH9, NAB2, NACC2, NCOA4, NFATC2, NPM1, NUTM1, PDGFRA, PDGFRB, PIK3CA, PAX3, PRKAR1A, RANBP2, SDC4, SEPTIN14, SLC34A2, SLC45A3, SS18, SSX2, STAT6, STRN, TACC3, TFG, TMPRSS2, TP53, TPM3, TRIM33, USP6
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