
Unbiased, deep sequencing of a nasal specimen from an otherwise healthy 13-month-old boy hospitalized in intensive care revealed high gene expression and the complete genome of a novel isolate of KI polyomavirus (KIPyV). Further investigation detected minimal gene expression of additional viruses, suggesting that KIPyV was potentially the causal agent. Analysis of the complete genome of isolate NMKI001 revealed it is different from all previously reported genomes and contains two amino acid differences as compared to the closest virus isolate, Stockholm 380 (EF127908). J. Med. Virol. 89:926-930, 2017. © 2016 Wiley Periodicals, Inc.
Male, Polyomavirus Infections, High-Throughput Nucleotide Sequencing, Infant, Sequence Homology, Genome, Viral, Sequence Analysis, DNA, Synteny, Cluster Analysis, Humans, Polyomavirus, Respiratory Tract Infections, Phylogeny
Male, Polyomavirus Infections, High-Throughput Nucleotide Sequencing, Infant, Sequence Homology, Genome, Viral, Sequence Analysis, DNA, Synteny, Cluster Analysis, Humans, Polyomavirus, Respiratory Tract Infections, Phylogeny
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 8 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
