病毒准种
康蒂格
水准点(测量)
计算机科学
路径(计算)
突变率
计算生物学
顺序装配
人口
基因组
突变
生物
遗传学
基因
大地测量学
基因表达
人口学
转录组
社会学
程序设计语言
地理
标识
DOI:10.1007/978-3-031-29119-7_1
摘要
Abstract With the high mutation rate in viruses, a mixture of closely related viral strains (called viral quasispecies) often co-infect an individual host. Reconstructing individual strains from viral quasispecies is a key step to characterizing the viral population, revealing strain-level genetic variability, and providing insights into biomedical and clinical studies. Reference-based approaches of reconstructing viral strains suffer from the lack of high-quality references due to high mutation rates and biased variant calling introduced by a selected reference. De novo methods require no references but face challenges due to errors in reads, the high similarity of quasispecies, and uneven abundance of strains. In this paper, we propose VStrains, a de novo approach for reconstructing strains from viral quasispecies. VStrains incorporates contigs, paired-end reads, and coverage information to iteratively extract the strain-specific paths from assembly graphs. We benchmark VStrains against multiple state-of-the-art de novo and reference-based approaches on both simulated and real datasets. Experimental results demonstrate that VStrains achieves the best overall performance on both simulated and real datasets under a comprehensive set of metrics such as genome fraction, duplication ratio, NGA50, error rate, etc . Availability: VStrains is freely available at https://github.com/ MetaGenTools/VStrains .
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