以个体杂合样本的单倍型形式对主要组织相容性复合体进行有针对性的全基因组测序

IF 6.2 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Genome research Pub Date : 2024-09-26 DOI:10.1101/gr.278588.123
Taishan Hu, Timothy L. Mosbruger, Nikolaos G. Tairis, Amalia Dinou, Pushkala Jayaraman, Mahdi Sarmady, Kingham Brewster, Yang Li, Tristan J. Hayeck, Jamie L. Duke, Dimitri S. Monos
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引用次数: 0

摘要

人类主要组织相容性复合物(MHC)是染色体 6 上一个约 4 Mb 的基因组片段,在免疫反应中起着关键作用。尽管它在各种性状和疾病中具有重要作用,但其复杂的性质使其在常规基础上进行准确表征具有挑战性。我们提出了一种新方法,利用长线程测序技术对杂合样本中的 MHC 区域进行有针对性的测序和全新的单倍型组装。我们使用两个参考样本、两个家庭三人组和一个非裔美国人样本对我们的方法进行了验证。我们对不同单倍型的覆盖率(96.6-99.9%,至少 30 倍深度)和准确率(99.89-99.99%)都非常高。该方法提供了一种可靠且经济有效的方法,无需进行全基因组测序即可对 MHC 进行测序并全面描述其特征,促进了对这一重要基因组片段的更广泛研究,在免疫学、遗传学和医学领域具有重要意义。
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Targeted and complete genomic sequencing of the Major Histocompatibility Complex in haplotypic form of individual heterozygous samples
The human Major Histocompatibility Complex (MHC) is an approximately 4 Mb genomic segment on Chromosome 6 that plays a pivotal role in the immune response. Despite its importance in various traits and diseases, its complex nature makes it challenging to accurately characterize on a routine basis. We present a novel approach allowing targeted sequencing and de novo haplotypic assembly of the MHC region in heterozygous samples, using long-read sequencing technologies. Our approach is validated using two reference samples, two family trios, and an African-American sample. We achieved excellent coverage (96.6-99.9% with at least 30× depth) and high accuracy (99.89-99.99%) for the different haplotypes. This methodology offers a reliable and cost-effective method for sequencing and fully characterizing the MHC without the need for whole-genome sequencing, facilitating broader studies on this important genomic segment and having significant implications in immunology, genetics and medicine.
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来源期刊
Genome research
Genome research 生物-生化与分子生物学
CiteScore
12.40
自引率
1.40%
发文量
140
审稿时长
6 months
期刊介绍: Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine. Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies. New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.
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