Search Result for: 使用22基因新一代测序面板分析骨髓增生性肿瘤的遗传变异

Analysis of Genetic Variants in Myeloproliferative Neoplasms Using a 22-Gene Next‑Generation Sequencing Panel

Analysis of Genetic Variants in Myeloproliferative Neoplasms Using a 22-Gene Next‑Generation Sequencing Panel

The Philadelphia (Ph)-negative myeloproliferative neoplasms (MPNs), namely essential thrombocythaemia (ET), polycythaemia vera (PV) and primary myelofibrosis (PMF), are a group of chronic clonal haematopoietic disorders that have the propensity to advance into bone marrow failure or acute myeloid leukaemia; often resulting in fatality. Although driver mutations have been identified in these MPNs, subtype-specific markers of the disease have yet to be discovered. Next-generation sequencing (NGS) technology can potentially improve the clinical management of MPNs by allowing for the simultaneous screening of many disease-associated genes.