ArticleNucleic acids research2010
Large-scale evolutionary surveillance of the 2009 H1N1 influenza A virus using resequencing arrays.
Article in Nucleic acids research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed.
- Whole genome sequence analysis of shallot virus X from India reveals it to be a natural recombinant with positive selection pressure.BMC genomic data · 2024Article
- Molecular features of influenza A (H1N1)pdm09 prevalent in Mexico during winter seasons 2012-2014.PloS one · 2017Article
- Pathogen chip for respiratory tract infections.Journal of clinical microbiology · 2013Article
- Variability among the neuraminidase, non-structural 1 and PB1-F2 proteins in the influenza A virus genome.Virus genes · 2012Review
- All that glitters is not gold--founder effects complicate associations of flu mutations to disease severity.Virology journal · 2010Article
- A metagenomic analysis of pandemic influenza A (2009 H1N1) infection in patients from North America.PloS one · 2010Article
- From complete genome sequence to 'complete' understanding?Trends in biotechnology · 2010Article
Corrections and comments
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Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In April 2009, a new influenza A (H1N1 2009) virus emerged that rapidly spread around the world. While current variants of this virus have caused widespread disease, particularly in vulnerable groups, there remains the possibility that future variants may cause increased virulence, drug resistance or vaccine escape. Early detection of these virus variants may offer the chance for increased containment and potentially prevention of the virus spread. We have developed and field-tested a resequencing kit that is capable of interrogating all eight segments of the 2009 influenza A(H1N1) virus genome and its variants, with added focus on critical regions such as drug-binding sites, structural components and mutation hotspots. The accompanying base-calling software (EvolSTAR) introduces novel methods that utilize neighbourhood hybridization intensity profiles and substitution bias of probes on the microarray for mutation confirmation and recovery of ambiguous base queries. Our results demonstrate that EvolSTAR is highly accurate and has a much improved call rate. The high throughput and short turn-around time from sample to sequence and analysis results (30 h for 24 samples) makes this kit an efficient large-scale evolutionary biosurveillance tool.
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Registered trials
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