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Histoimmunogenetics Markup Language 1.0: Reporting next generation sequencing-based HLA and KIR genotyping

机译:组织免疫遗传学标记语言1.0:报告基于下一代测序的HLA和KIR基因分型

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摘要

We present an electronic format for exchanging data for HLA and KIR genotyping with extensions for next-generation sequencing (NGS). This format addresses NGS data exchange by refining the Histoimmunogenetics Markup Language (HML) to conform to the proposed Minimum Information for Reporting Immunogenomic NGS Genotyping (MIRING) reporting guidelines (miring.immunogenomics. org). Our refinements of HML include two major additions. First, NGS is supported by new XML structures to capture additional NGS data and metadata required to produce a genotyping result, including analysis-dependent (dynamic) and method-dependent (static) components. A full genotype, consensus sequence, and the surrounding metadata are included directly, while the raw sequence reads and platform documentation are externally referenced. Second, genotype ambiguity is fully represented by integrating Genotype List Strings, which use a hierarchical set of delimiters to represent allele and genotype ambiguity in a complete and accurate fashion. HML also continues to enable the transmission of legacy methods (e.g. site-specific oligonucleotide, sequence-specific priming, and Sequence Based Typing (SBT)), adding features such as allowing multiple group-specific sequencing primers, and fully leveraging techniques that combine multiple methods to obtain a single result, such as SBT integrated with NGS. (C) 2015 The Authors. Published by Elsevier Inc. on behalf of American Society for Histocompatibility and Immunogenetics.
机译:我们提出了一种电子格式,用于交换HLA和KIR基因分型的数据,并扩展了下一代测序(NGS)。此格式通过改进组织免疫遗传学标记语言(HML)来满足建议的报告免疫基因组NGS基因分型的最低信息(MIRING)报告指南(miring.immunogenomics.org)来解决NGS数据交换问题。我们对HML的改进包括两个主要方面。首先,新的XML结构支持NGS捕获生成基因分型结果所需的其他NGS数据和元数据,包括依赖于分析的(动态)和依赖于方法的(静态)组件。直接包含完整的基因型,共有序列和周围的元数据,而外部序列则引用了原始序列读数和平台文档。其次,通过整合基因型列表字符串,可以充分体现基因型歧义,该字符串使用分层定界符集以完整,准确的方式表示等位基因和基因型歧义。 HML还继续支持传统方法的传递(例如位点特异性寡核苷酸,序列特异性引物和基于序列的键入(SBT)),添加了诸如允许多个组特异性测序引物之类的功能,以及将多种获得单个结果的方法,例如SBT与NGS集成。 (C)2015作者。由Elsevier Inc.代表美国组织相容性和免疫遗传学学会出版。

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