Please use this identifier to cite or link to this item:
https://doi.org/10.1186/s12864-017-3714-6
DC Field | Value | |
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dc.title | A universal genome sequencing method for rotavirus A from human fecal samples which identifies segment reassortment and multi-genotype mixed infection | |
dc.contributor.author | Dung T.T.N. | |
dc.contributor.author | Duy P.T. | |
dc.contributor.author | Sessions O.M. | |
dc.contributor.author | Sangumathi U.K. | |
dc.contributor.author | Phat V.V. | |
dc.contributor.author | Tam P.T.T. | |
dc.contributor.author | To N.T.N. | |
dc.contributor.author | Phuc T.M. | |
dc.contributor.author | Hong Chau T.T. | |
dc.contributor.author | Chau N.N.M. | |
dc.contributor.author | Minh N.N. | |
dc.contributor.author | Thwaites G.E. | |
dc.contributor.author | Rabaa M.A. | |
dc.contributor.author | Baker S. | |
dc.date.accessioned | 2020-09-01T07:55:34Z | |
dc.date.available | 2020-09-01T07:55:34Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Dung T.T.N., Duy P.T., Sessions O.M., Sangumathi U.K., Phat V.V., Tam P.T.T., To N.T.N., Phuc T.M., Hong Chau T.T., Chau N.N.M., Minh N.N., Thwaites G.E., Rabaa M.A., Baker S. (2017). A universal genome sequencing method for rotavirus A from human fecal samples which identifies segment reassortment and multi-genotype mixed infection. BMC Genomics 18 (1) : 324. ScholarBank@NUS Repository. https://doi.org/10.1186/s12864-017-3714-6 | |
dc.identifier.issn | 14712164 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/173848 | |
dc.description.abstract | Background: Genomic characterization of rotavirus (RoV) has not been adopted at large-scale due to the complexity of obtaining sequences for all 11 segments, particularly when feces are used as starting material. Methods: To overcome these limitations, we developed a novel RoV capture and genome sequencing method combining commercial enzyme immunoassay plates and a set of routinely used reagents. Results: Our approach had a 100% success rate, producing >90% genome coverage for diverse RoV present in fecal samples (Ct < 30). Conclusions: This method provides a novel, reproducible and comparatively simple approach for genomic RoV characterization and could be scaled-up for use in global RoV surveillance systems. Trial registration (prospectively registered): Current Controlled Trials ISRCTN88101063. Date of registration: 14/06/2012 © 2017 The Author(s). | |
dc.publisher | BioMed Central Ltd. | |
dc.source | Unpaywall 20200831 | |
dc.subject | Article | |
dc.subject | child | |
dc.subject | enzyme immunoassay | |
dc.subject | feces analysis | |
dc.subject | gene amplification | |
dc.subject | genetic reassortment | |
dc.subject | human | |
dc.subject | mixed infection | |
dc.subject | nonhuman | |
dc.subject | nucleic acid amplification | |
dc.subject | nucleotide sequence | |
dc.subject | phylogeny | |
dc.subject | randomized controlled trial (topic) | |
dc.subject | RNA extraction | |
dc.subject | Rotavirus A | |
dc.subject | Rotavirus infection | |
dc.subject | sequence analysis | |
dc.subject | unindexed sequence | |
dc.subject | virus genome | |
dc.subject | virus load | |
dc.subject | virus purification | |
dc.subject | feces | |
dc.subject | genetic reassortment | |
dc.subject | genetics | |
dc.subject | genomics | |
dc.subject | genotype | |
dc.subject | physiology | |
dc.subject | procedures | |
dc.subject | Rotavirus | |
dc.subject | virology | |
dc.subject | virus genome | |
dc.subject | complementary DNA | |
dc.subject | DNA, Complementary | |
dc.subject | Feces | |
dc.subject | Genome, Viral | |
dc.subject | Genomics | |
dc.subject | Genotype | |
dc.subject | Humans | |
dc.subject | Phylogeny | |
dc.subject | Reassortant Viruses | |
dc.subject | Rotavirus | |
dc.subject | Sequence Analysis, RNA | |
dc.subject | Viral Load | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS MEDICAL SCHOOL | |
dc.description.doi | 10.1186/s12864-017-3714-6 | |
dc.description.sourcetitle | BMC Genomics | |
dc.description.volume | 18 | |
dc.description.issue | 1 | |
dc.description.page | 324 | |
dc.published.state | Published | |
Appears in Collections: | Elements Staff Publications |
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