Suppr超能文献

用于危重症婴儿三联快速基因组测序的集成流程

An Integrated Pipeline for Trio-Rapid Genome Sequencing in Critically Ill Infants.

作者信息

Wang Xiao, Gan Mingyu, Dong Xinran, Lu Yulan, Zhou Wenhao

机构信息

Center for Molecular Medicine, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.

Center for Big Data in Clinical Research, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.

出版信息

Curr Protoc. 2023 Mar;3(3):e706. doi: 10.1002/cpz1.706.

Abstract

Trio-rapid genome sequencing (trio-rGS) can assist the genetic diagnosis of critically ill infants given its ability to detect a broad range of pathogenic variants, as well as microbes, simultaneously with high efficiency. To achieve more comprehensive clinical diagnoses, it is essential to propose a recommended protocol in clinical practice. Here, we introduced an integrated pipeline to detect germline variants and microorganisms simultaneously from trio-RGS in critically ill infants, which provides step-by-step criteria for the semi-automatic processing procedures. With this pipeline in clinical application, only 1 ml of peripheral blood is needed for clinicians to provide both genetic and infectious causal information to a patient. The establishment and clinical practice of the method is of great significance for further mining of high-throughput sequencing data and for assisting clinicians in promoting diagnosis efficiency and accuracy. © 2023 Wiley Periodicals LLC. Basic Protocol 1: Experimental pipeline for rapid whole-genome sequencing for the simultaneous detection of germline variants and microorganisms Basic Protocol 2: Computational pipeline for rapid whole-genome sequencing for the simultaneous detection of germline variants and microorganisms.

摘要

三联快速基因组测序(trio-rGS)能够高效地同时检测广泛的致病变异以及微生物,有助于对危重症婴儿进行基因诊断。为了实现更全面的临床诊断,在临床实践中提出推荐方案至关重要。在此,我们介绍了一种综合流程,可从危重症婴儿的三联RGS中同时检测种系变异和微生物,该流程为半自动处理程序提供了逐步标准。通过在临床应用中采用此流程,临床医生仅需1毫升外周血,就能为患者提供遗传和感染病因信息。该方法的建立和临床实践对于进一步挖掘高通量测序数据以及协助临床医生提高诊断效率和准确性具有重要意义。© 2023威利期刊有限责任公司。基本方案1:用于同时检测种系变异和微生物的快速全基因组测序实验流程 基本方案2:用于同时检测种系变异和微生物的快速全基因组测序计算流程。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验