Beijing Key Laboratory for Genetics of Birth Defects, Beijing Pediatric Research Institute; MOE Key Laboratory of Major Diseases in Children; Rare Disease Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Institute of Biomedical Engineering, University of Toronto, Toronto, M5S 3G9, Canada.
Genomics Proteomics Bioinformatics. 2024 Jul 3;22(2). doi: 10.1093/gpbjnl/qzad007.
Single-cell RNA sequencing (scRNA-seq) has emerged as a valuable tool for studying cellular heterogeneity in various fields, particularly in virological research. By studying the viral and cellular transcriptomes, the dynamics of viral infection can be investigated at a single-cell resolution. However, limited studies have been conducted to investigate whether RNA transcripts from clinical samples contain substantial amounts of viral RNAs, and a specific computational framework for efficiently detecting viral reads based on scRNA-seq data has not been developed. Hence, we introduce DVsc, an open-source framework for precise quantitative analysis of viral infection from single-cell transcriptomics data. When applied to approximately 200 diverse clinical samples that were infected by more than 10 different viruses, DVsc demonstrated high accuracy in systematically detecting viral infection across a wide array of cell types. This innovative bioinformatics pipeline could be crucial for addressing the potential effects of surreptitiously invading viruses on certain illnesses, as well as for designing novel medicines to target viruses in specific host cell subsets and evaluating the efficacy of treatment. DVsc supports the FASTQ format as an input and is compatible with multiple single-cell sequencing platforms. Moreover, it could also be applied to sequences from bulk RNA sequencing data. DVsc is available at http://62.234.32.33:5000/DVsc.
单细胞 RNA 测序 (scRNA-seq) 已成为研究各个领域细胞异质性的重要工具,特别是在病毒学研究中。通过研究病毒和细胞转录组,可以在单细胞分辨率下研究病毒感染的动态。然而,目前还很少有研究调查临床样本中的 RNA 转录本是否含有大量的病毒 RNA,也没有开发出特定的基于 scRNA-seq 数据的高效检测病毒读段的计算框架。因此,我们引入了 DVsc,这是一个用于从单细胞转录组学数据中精确定量分析病毒感染的开源框架。当应用于大约 200 个由超过 10 种不同病毒感染的多样化临床样本时,DVsc 在系统地检测广泛的细胞类型中的病毒感染方面表现出了很高的准确性。这种创新的生物信息学管道对于解决隐匿性入侵病毒对某些疾病的潜在影响,以及设计针对特定宿主细胞亚群的病毒的新型药物和评估治疗效果可能至关重要。DVsc 支持 FASTQ 格式作为输入,与多个单细胞测序平台兼容。此外,它还可以应用于批量 RNA 测序数据的序列。DVsc 可在 http://62.234.32.33:5000/DVsc 上获得。