Latest Implications of Next-Gen Sequencing in Diagnosis of Acute and Chronic Myeloid Leukemia

O. Boldura, Cristina Petrine, A. Mihu, C. Baltă
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Abstract

The spectacular progress which was present in the past few years in the field of genome sequencing, together with the appearance on the market of some high performance devices in this field, the reduction of the costs regarding the analysis of the samples and the standardization of some protocols, has led to the establishment and introduction of the new generation of sequencing techniques in clinical diagnostic labs. An important role is played by the implementation of this technique in the oncology clinics. In this context, we found it appropriate to discuss in this chapter about the role of next-gen sequencing in determining the genetic probabili-ties of occurrence of oncological pathologies in the healthy population, the screen-ing of these diseases at the population level, the diagnosis and classification of this pathology, the establishment of the therapeutic conduct using the technique, as well as the progression of the disease. In this chapter, we intend to discuss in particular the involvement of this technology in hemato-oncological diseases.
新一代测序在急性和慢性髓系白血病诊断中的最新意义
在过去的几年中,基因组测序领域取得了惊人的进展,随着该领域一些高性能设备在市场上的出现,样品分析成本的降低和一些协议的标准化,导致了新一代测序技术在临床诊断实验室的建立和引入。该技术在肿瘤临床中发挥着重要作用。在这种情况下,我们认为在本章中讨论下一代测序在确定健康人群中肿瘤病理发生的遗传概率、在人群水平上筛查这些疾病、诊断和分类这种病理、使用该技术建立治疗行为以及疾病进展方面的作用是合适的。在本章中,我们打算特别讨论这项技术在血液肿瘤疾病中的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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