2015
DOI: 10.1016/j.jviromet.2014.09.020
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Sequencing human rhinoviruses: Direct sequencing versus plasmid cloning

Abstract: Human rhinoviruses (RV) are associated with the majority of viral respiratory illnesses in infants, children and adults. Over the last several years, researchers have begun to sequence the many different species and strains of RV in order to determine if certain species were associated with increased disease severity. There are a variety of techniques employed to prepare samples for sequencing. One method utilizes plasmid-cloning, which is expensive and takes several hours to complete. Recently, some investiga… Show more

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Cited by 2 publications
(2 citation statements)
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“…42 Samples positive for RV were then cloned and sequenced. A 548-nucleotide sequence that encompassed the VP4/VP2 region 51 was amplified, directly sequenced, 45 and compared with published GenBank sequences to determine species. MPV and RSV were tested for by RT-PCR using primers/probes previously described.…”
Section: Samplesmentioning
confidence: 99%
“…42 Samples positive for RV were then cloned and sequenced. A 548-nucleotide sequence that encompassed the VP4/VP2 region 51 was amplified, directly sequenced, 45 and compared with published GenBank sequences to determine species. MPV and RSV were tested for by RT-PCR using primers/probes previously described.…”
Section: Samplesmentioning
confidence: 99%
“…It should be noted that previous research has reported failure rates for both methods. 45 Therefore, the selection of the most efficient and cost-effective approach to investigate the methylation pattern depends on the study question and design, as well as the information provided by each method. In this study, we used a site-specific assessment method, facilitating a rapid and direct investigation of the methylation status.…”
Section: Gene Symbol (Ensembl Accession Number)mentioning
confidence: 99%