檢驗方法：
次世代定序 (Next Generation Sequencing, NGS)
生物參考區間(REFERENCE RANGE)：不適用
干擾物質：
臨床意義 or 實驗室解釋：
基因檢測(64基因)
1. 檢測標的：ABL1, ALK, ASXL1, BCL2, BCOR, BRAF, CALR, CBL, CCND1, CEBPA, CREBBP, CSF3R, DNMT3A, EGFR,ETV6,EZH2, FGFR1, FGFR2, FLT3, FUS, GATA2, HMGA2, HRAS, IDH1, IDH2, IKZF1, JAK2, KIT, KMT2A, KRAS, MECOM, MET, MLLT10, MLLT3, MPL, MYBL1, MYD88, MYH11, NF1, NPM1, NRAS, NTRK3, NUP214, PDGFRA, PDGFRB, PHF6, PRPF8, PTPN11, RARA, RB1, RBM15, RUNX1, SETBP1, SF3B1, SH2B3, SRSF2, STAG2, TCF3, TET2, TFE3, TP53, U2AF1, WT1, ZRSR2
2. 數據判讀：單點變異(Single Nucleotide Variant, SNV)、片段插入或缺失(Insertion or Deletion, InDel)與基因融合(fusion gene)。