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The rare and undiagnosed diseases diagnostic service – application of massively parallel sequencing in a state-wide clinical service

机译:罕见且未经诊断的疾病诊断服务–大规模并行测序在全州临床服务中的应用

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摘要

BackgroundThe Rare and Undiagnosed Diseases Diagnostic Service (RUDDS) refers to a genomic diagnostic platform operating within the Western Australian Government clinical services delivered through Genetic Services of Western Australia (GSWA). GSWA has provided a state-wide service for clinical genetic care for 28 years and it serves a population of 2.5 million people across a geographical area of 2.5milion Km2. Within this context, GSWA has established a clinically integrated genomic diagnostic platform in partnership with other public health system managers and service providers, including but not limited to the Office of Population Health Genomics, Diagnostic Genomics (PathWest Laboratories) and with executive level support from the Department of Health. Herein we describe report presents the components of this service that are most relevant to the heterogeneity of paediatric clinical genetic care.
机译:背景罕见病和未诊断疾病诊断服务(RUDDS)是指在西澳大利亚州政府通过西澳大利亚州遗传服务(GSWA)提供的临床服务中运行的基因组诊断平台。 GSWA为临床遗传护理提供了全州范围的服务,已有28年的历史,它为250万人口提供服务,覆盖250万人口Km 2 。在此背景下,GSWA与其他公共卫生系统管理人员和服务提供商建立了临床上集成的基因组诊断平台,包括但不限于人口健康基因组学,诊断基因组学办公室(PathWest实验室),并获得了行政部门的支持健康部门。在这里,我们描述的报告提出了与儿童临床遗传保健异质性最相关的这项服务的组成部分。

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