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下一代测序技术对荷兰注册人群中的 HLA 多样性进行了特征描述。

Next generation sequencing characterizes HLA diversity in a registry population from the Netherlands.

机构信息

CW Bill Young Marrow Donor Recruitment and Research Program, Departments of Pediatrics and Oncology, Georgetown University, Washington, District of Columbia.

Matchis Foundation, Leiden, The Netherlands.

出版信息

HLA. 2019 Jun;93(6):474-483. doi: 10.1111/tan.13535. Epub 2019 Apr 4.

Abstract

Next generation DNA sequencing is used to determine the HLA-A, -B, -C, -DRB1, -DRB3/4/5, and -DQB1 assignments of 1009 unrelated volunteers for the unrelated donor registry in The Netherlands. The analysis characterizes all HLA exons and introns for class I alleles; at least exons 2 to 3 for HLA-DRB1; and exons 2 to 6 for HLA-DQB1. Of the distinct alleles present, there are 229 class I and 71 class II; 36 of these alleles are novel. The majority (approximately 98%) of the cumulative allele frequency at each locus is contributed by alleles that appear three or more times. Alleles encoding protein variation outside of the antigen recognition domains are 0.6% of the class I assignments and 5.3% of the class II assignments.

摘要

下一代 DNA 测序用于确定荷兰无关供体登记处的 1009 名无关志愿者的 HLA-A、-B、-C、-DRB1、-DRB3/4/5 和 -DQB1 分配。该分析对所有 HLA 外显子和内含子进行了分类 I 等位基因的特征描述;至少对 HLA-DRB1 进行了外显子 2 到 3 的分析;对 HLA-DQB1 进行了外显子 2 到 6 的分析。在存在的独特等位基因中,有 229 个 I 类和 71 个 II 类;其中 36 个是新的。每个基因座的累积等位基因频率中,约有 98%是由出现三次或更多次的等位基因贡献的。在抗原识别结构域外编码蛋白质变异的等位基因占 I 类分配的 0.6%,占 II 类分配的 5.3%。

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