Additional file 1 of Identification of a novel HOOK3-FGFR1 fusion gene involved in activation of the NF-kappaB pathway

Additional file 1: Table S1. Clinical and laboratory characteristics of the 20 MDS patients. Table S2. A panel of 38 commonly mutated genes in myeloid hematologic malignancies. Table S3. Mutations detected by the target panel or WES in the MDS patients. Table S4. Gene fusions detected by STAR-Fusion in the 20 MDS patients. Table S5. Differentially expressed genes from the comparison between the HOOK3-FGFR1 positive patient and healthy donors

附加文件1：表S1。20例骨髓增生异常综合征（Myelodysplastic Syndromes, MDS）患者的临床与实验室特征。表S2。髓系血液恶性肿瘤中38个常见突变基因的靶标检测面板。表S3。该20例骨髓增生异常综合征患者经靶标基因面板或全外显子测序（Whole Exome Sequencing, WES）检测得到的突变信息。表S4。该20例骨髓增生异常综合征患者经STAR-Fusion工具检测到的基因融合事件。表S5。HOOK3-FGFR1阳性患者与健康对照个体转录组比较分析所得的差异表达基因。