2012
DOI: 10.1586/erm.12.67
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Is next-generation sequencing an important tool in HPV subtype diagnosis?

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Cited by 4 publications
(5 citation statements)
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“…In addition, reported methods based on PCR-Sanger sequencing generally require prior knowledge of the infecting HPV type since they use HPV type-specific primers for PCR [ 9 , 10 ]. These technical hurdles can be overcome by using massively parallel high-throughput sequencing (or NGS, next-generation sequencing) technologies, which allow sequencing of multiple HPV types and variants in clinical specimens and the identification of minority genetic variants in individual samples [ 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ]. Reported NGS-based methods for HPV detection and typing consisted either in deep sequencing of amplicons obtained from the amplification of highly conserved regions in HPV genome or in the unbiased metagenomics sequencing of whole DNA or RNA from biological samples.…”
Section: Introductionmentioning
confidence: 99%
“…In addition, reported methods based on PCR-Sanger sequencing generally require prior knowledge of the infecting HPV type since they use HPV type-specific primers for PCR [ 9 , 10 ]. These technical hurdles can be overcome by using massively parallel high-throughput sequencing (or NGS, next-generation sequencing) technologies, which allow sequencing of multiple HPV types and variants in clinical specimens and the identification of minority genetic variants in individual samples [ 20 , 21 , 22 , 23 , 24 , 25 , 26 , 27 , 28 , 29 ]. Reported NGS-based methods for HPV detection and typing consisted either in deep sequencing of amplicons obtained from the amplification of highly conserved regions in HPV genome or in the unbiased metagenomics sequencing of whole DNA or RNA from biological samples.…”
Section: Introductionmentioning
confidence: 99%
“…The increasing clinical requirements for accurate virus typing are therefore likely to play a fundamental role in how future HPV detection techniques become adopted [17]. NGS can be used to measure viral load and subtype, as well as providing a map of large-scale chromosomal damage [16].…”
Section: Next Generation Sequencing In the Hpv Fieldmentioning
confidence: 99%
“…Although currently more of a research method than a diagnostic assay, as the cost of sequencing decreases, NGS may become a useful technique giving information about genomic integration. The low-coverage genomic sequencing approach will give information about viral load and subtype, as well as genomic copy number patterns, which in turn could suggest whether the disease has a HPV-typical genome or one associated with other etiological factors, and aid clinical decision-making in the future [17]. Future developments are also bound to impact clinical decision-making.…”
Section: Next Generation Sequencing In the Hpv Fieldmentioning
confidence: 99%
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