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

补充材料1：表S1。20例骨髓增生异常综合征（Myelodysplastic Syndromes, MDS）患者的临床及实验室特征。表S2。髓系血液系统恶性肿瘤中38个常见突变基因的靶向检测面板。表S3。通过靶向测序面板或全外显子组测序（Whole Exome Sequencing, WES）在MDS患者中检测到的突变。表S4。20例MDS患者中通过STAR-Fusion工具检测到的基因融合事件。表S5。HOOK3-FGFR1阳性患者与健康供体的对照比较中筛选得到的差异表达基因。