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A Method for Hypermutated Viral Sequences Detection in Fastq and Bam Format Files

机译:Fastq和Bam格式文件中的超变异病毒序列检测方法

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Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like3 (APOBEC3), is a well characterized enzyme that attacks virus genome replication cycle such as HIV, SIV, HBV, leading context dependent G-to-A changes, referred to as "hypermutation." Several methods have analyzed and described these hypermutation sites by aligning affected sequences to a reference sequence. In our previous study, we demonstrated that indels (insertions/deletions) in the sequences lead to an incorrect assignment of APOBEC3 targeted and non-target sites which can result in an incorrect identification of hypermutated sequences and erroneous biological inferences made based on hypermutation analysis. To date, several approaches have been developed in order to analysis of hypermutated sequences, yet no method has been developed to detect hypermutated reads in fastq and bam formats files. In this study, we propose a suitable method based on our recent proposed method (G2A3) that can identify hypermutated reads in fastq and bam formats datasets.
机译:载脂蛋白B mRNA编辑酶,催化性多肽样3(APOBEC3),是一种特征明确的酶,可攻击病毒基因组复制周期,例如HIV,SIV,HBV,从而导致上下文相关的G到A改变,称为“超突变”。通过将受影响的序列与参考序列比对,几种方法已经分析和描述了这些超突变位点。在我们先前的研究中,我们证明了序列中的插入/缺失(插入/缺失)导致对APOBEC3目标和非目标位点的错误分配,这可能导致对超突变序列的错误识别以及基于超突变分析做出的错误生物学推论。迄今为止,已经开发了几种方法来分析超突变序列,但是还没有开发出用于检测fastq和bam格式文件中的超突变读段的方法。在这项研究中,我们基于最近提出的方法(G2A3)提出了一种合适的方法,该方法可以识别fastq和bam格式数据集中的超突变读取。

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