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VANIR—NextFlow Pipeline for Viral Variant Calling and de Novo Assembly of Nanopore and Illumina Reads for High-Quality dsDNA Viral Genomes

机译:Vanir-nextflow管道用于病毒变体呼叫和纳米孔和Illumina的De Novo集装读取高质量DSDNA病毒基因组

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Human cytomegalovirus (HCMV), like other herpes and dsDNA viruses, possesses unique properties derived from their genome architecture. The HCMV genome is composed of two unique domains: long (L) and short (S). Each domain contains a central unique region (U; thus, UL and US, respectively) and two repeated regions (thus, TRL/IRL and TRS/IRS). Recombination between repetitive regions is possible, yielding four possible genomic isomers, found in equimolar proportion in any viral infective population. Frequent recombination and an altered selective landscape can give rise to the persistence, if not fixation, of diverse variants in culturized HCMV isolates. This phenomenon has already been discovered in AD169 and Towne strains, characterizing a 10 kbp deletion (ΔUL/b’) in commonly used viral strains. Other dsDNA viruses are known for their structural rearrangements and frequent recombination. VANIR (viral variant calling and de novo assembly using nanopore and illumina reads) is a novel analysis pipeline that benefits from both short-read (Illumina) and long-read sequencing technologies (Oxford Nanopore Technologies Ltd.) to assemble high-quality dsDNA viral genomes and detection of variants. Illumina and nanopore sequencing provide complementary information to the assembly and variant discovery. Assembly contiguity, structural variant, and repeat calling are greatly improved by nanopore read-length and base-calling and base confidence by Illumina reduced error rate and increased yield. This specialized bioinformatic analysis pipeline is encoded in the NextFlow pipeline manager and containerized in a Singularity image. This set-up allows for improved traceability, reproducibility, transportability, and speed. Through VANIR, novel point mutations and structural genome rearrangements are called from sequencing data, benefiting diversity research with attenuated lab-strains and wild-type viruses.
机译:与其他疱疹和DSDNA病毒一样,人巨细胞病毒(HCMV)具有来自其基因组结构的独特性质。 HCMV基因组由两个独特的结构域组成:长(L)和短(S)。每个域包含一个中心唯一区域(U;因此,UL和美国)和两个重复区域(因此,TRL / IRL和TRS / IRS)。可以在任何病毒感染群体中以等摩尔比例发现四种可能的基因组异构体之间的重组。频繁的重组和改变的选择性景观可以引起培养的HCMV分离株中不同变体的持久性,如果没有固定。这种现象已经在Ad169和Towne菌株中发现,其特征在常用的病毒菌株中,表征了10kbp缺失(δ ul / b’)。其他DSDNA病毒以其结构重排和频繁的重组而闻名。 Vanir(使用纳米孔和Illumina读取的病毒变体呼叫和De Novo组装)是一种新颖的分析管道,其益处短读(Illumina)和长读测序技术(牛津纳米孔技术有限公司)益处,以组装高质量的DSDNA病毒基因组和变体检测。 Illumina和Nanopore测序为大会和变体发现提供了互补信息。通过纳米孔读取长度和基本呼叫和基本置信度降低误差率和增加的产量,大大提高了续集,结构变体和重复呼叫。该专业的生物信息分析管道在NextFlow Pipeline Manager中编码,并在奇点图像中容化。该设置允许改进的可追溯性,再现性,可运输性和速度。通过Vanir,从测序数据中调用新的点突变和结构基因组重排,利益与减毒的实验室和野生型病毒的多样性研究。

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