PCIP-seq:整合病毒基因组及其插入位点的同时测序。

IF 12.3 1区 生物学 Q1 Agricultural and Biological Sciences
Maria Artesi, Vincent Hahaut, Basiel Cole, Laurens Lambrechts, Fereshteh Ashrafi, Ambroise Marçais, Olivier Hermine, Philip Griebel, Natasa Arsic, Frank van der Meer, Arsène Burny, Dominique Bron, Elettra Bianchi, Philippe Delvenne, Vincent Bours, Carole Charlier, Michel Georges, Linos Vandekerckhove, Anne Van den Broeke, Keith Durkin
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引用次数: 20

摘要

病毒基因组与宿主基因组的整合对受感染细胞的轨迹有重大影响。相关病毒基因组内的整合位置和变异可以影响感染细胞的克隆扩增和持久性。基于短读测序的方法可以识别病毒插入位点,但其内病毒基因组的序列尚不清楚。我们开发了PCIP-seq,这是一种利用长读数来识别插入位点并对其相关病毒基因组进行测序的方法。我们将该技术应用于外源性逆转录病毒HTLV-1、BLV和HIV-1、内源性逆转录病毒和人乳头瘤病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

PCIP-seq: simultaneous sequencing of integrated viral genomes and their insertion sites with long reads.

PCIP-seq: simultaneous sequencing of integrated viral genomes and their insertion sites with long reads.

PCIP-seq: simultaneous sequencing of integrated viral genomes and their insertion sites with long reads.

PCIP-seq: simultaneous sequencing of integrated viral genomes and their insertion sites with long reads.

The integration of a viral genome into the host genome has a major impact on the trajectory of the infected cell. Integration location and variation within the associated viral genome can influence both clonal expansion and persistence of infected cells. Methods based on short-read sequencing can identify viral insertion sites, but the sequence of the viral genomes within remains unobserved. We develop PCIP-seq, a method that leverages long reads to identify insertion sites and sequence their associated viral genome. We apply the technique to exogenous retroviruses HTLV-1, BLV, and HIV-1, endogenous retroviruses, and human papillomavirus.

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来源期刊
Genome Biology
Genome Biology BIOTECHNOLOGY & APPLIED MICROBIOLOGY-GENETICS & HEREDITY
CiteScore
25.50
自引率
3.30%
发文量
0
审稿时长
14 weeks
期刊介绍: Genome Biology is a leading research journal that focuses on the study of biology and biomedicine from a genomic and post-genomic standpoint. The journal consistently publishes outstanding research across various areas within these fields. With an impressive impact factor of 12.3 (2022), Genome Biology has earned its place as the 3rd highest-ranked research journal in the Genetics and Heredity category, according to Thomson Reuters. Additionally, it is ranked 2nd among research journals in the Biotechnology and Applied Microbiology category. It is important to note that Genome Biology is the top-ranking open access journal in this category. In summary, Genome Biology sets a high standard for scientific publications in the field, showcasing cutting-edge research and earning recognition among its peers.
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