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Highlighting Clinical Metagenomics for Enhanced Diagnostic Decision-making: A Step Towards Wider Implementation

机译:突出临床基因组学以增强诊断决策能力:迈向更广泛实施的一步

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摘要

Clinical metagenomics (CMg) is the discipline that refers to the sequencing of all nucleic acid material present within a clinical specimen with the intent to recover clinically relevant microbial information. From a diagnostic perspective, next-generation sequencing (NGS) offers the ability to rapidly identify putative pathogens and predict their antimicrobial resistance profiles to optimize targeted treatment regimens. Since the introduction of metagenomics nearly a decade ago, numerous reports have described successful applications in an increasing variety of biological specimens, such as respiratory secretions, cerebrospinal fluid, stool, blood and tissue. Considerable advancements in sequencing and computational technologies in recent years have made CMg a promising tool in clinical microbiology laboratories. Moreover, costs per sample and turnaround time from specimen receipt to clinical management continue to decrease, making the prospect of CMg more feasible. Many difficulties, however, are associated with CMg and warrant further improvements such as the informatics infrastructure and analytical pipelines. Thus, the current review focuses on comprehensively assessing applications of CMg for diagnostic and subtyping purposes.
机译:临床宏基因组学(CMg)是指对临床标本中存在的所有核酸材料进行测序以恢复临床相关微生物信息的学科。从诊断的角度来看,下一代测序(NGS)提供了快速识别推定病原体并预测其抗菌素耐药性以优化目标治疗方案的能力。自从近十年前引入宏基因组学技术以来,许多报道已经描述了在越来越多的生物学标本中的成功应用,例如呼吸道分泌物,脑脊液,粪便,血液和组织。近年来,测序和计算技术的显着进步使CMg成为临床微生物学实验室中有希望的工具。而且,每个样品的成本以及从标本接收到临床管理的周转时间持续减少,这使得CMg的前景更加可行。但是,许多困难与CMg有关,需要进一步改进,例如信息学基础架构和分析管道。因此,本综述着重于全面评估CMg在诊断和亚型分析中的应用。

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