Venus: An efficient virus infection detection and fusion site discovery method using single-cell and bulk RNA-seq data.
Venus: An efficient virus infection detection and fusion site discovery method using single-cell and bulk RNA-seq data.
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DOI:
10.1371/journal.pcbi.1010636
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发表时间:
2022-10
影响因子:
4.3
通讯作者:
中科院分区:
文献类型:
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作者:
Early and accurate detection of viruses in clinical and environmental samples is essential for effective public healthcare, treatment, and therapeutics. While PCR detects potential pathogens with high sensitivity, it is difficult to scale and requires knowledge of the exact sequence of the pathogen. With the advent of next-gen single-cell sequencing, it is now possible to scrutinize viral transcriptomics at the finest possible resolution–cells. This newfound ability to investigate individual cells opens new avenues to understand viral pathophysiology with unprecedented resolution. To leverage this ability, we propose an efficient and accurate computational pipeline, named Venus, for virus detection and integration site discovery in both single-cell and bulk-tissue RNA-seq data. Specifically, Venus addresses two main questions: whether a tissue/cell type is infected by viruses or a virus of interest? And if infected, whether and where has the virus inserted itself into the human genome? Our analysis can be broken into two parts–validation and discovery. Firstly, for validation, we applied Venus on well-studied viral datasets, such as HBV- hepatocellular carcinoma and HIV-infection treated with antiretroviral therapy. Secondly, for discovery, we analyzed datasets such as HIV-infected neurological patients and deeply sequenced T-cells. We detected viral transcripts in the novel target of the brain and high-confidence integration sites in immune cells. In conclusion, here we describe Venus, a publicly available software which we believe will be a valuable virus investigation tool for the scientific community at large.
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DOI:
10.1007/978-1-4939-3572-7_13
发表时间:
2016-01-01
期刊:
DATA MINING TECHNIQUES FOR THE LIFE SCIENCES
影响因子:
--
作者:
Dobin, Alexander;Gingeras, Thomas R.
通讯作者:
Gingeras, Thomas R.
影响因子:
7.3
作者:
Marban C;Forouzanfar F;Ait-Ammar A;Fahmi F;El Mekdad H;Daouad F;Rohr O;Schwartz C
通讯作者:
Schwartz C
影响因子:
5.2
作者:
Kazachenka A;Kassiotis G
通讯作者:
Kassiotis G
影响因子:
16.6
作者:
Zheng GX;Terry JM;Belgrader P;Ryvkin P;Bent ZW;Wilson R;Ziraldo SB;Wheeler TD;McDermott GP;Zhu J;Gregory MT;Shuga J;Montesclaros L;Underwood JG;Masquelier DA;Nishimura SY;Schnall-Levin M;Wyatt PW;Hindson CM;Bharadwaj R;Wong A;Ness KD;Beppu LW;Deeg HJ;McFarland C;Loeb KR;Valente WJ;Ericson NG;Stevens EA;Radich JP;Mikkelsen TS;Hindson BJ;Bielas JH
通讯作者:
Bielas JH
影响因子:
4.9
作者:
Benachenhou F;Sperber GO;Bongcam-Rudloff E;Andersson G;Boeke JD;Blomberg J
通讯作者:
Blomberg J