Evidence map›Paper›PMID 27974548›Full record

ArticleJournal of clinical microbiology2017

Universal Human Papillomavirus Typing Assay: Whole-Genome Sequencing following Target Enrichment.

Tengguo Li, Elizabeth R Unger, Dhwani Batra, Mili Sheth, Martin Steinau, Jean Jasinski, Jennifer Jones, Mangalathu S Rajeevan

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Journal of clinical microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 19 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Tengguo LiDivision of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Elizabeth R UngerDivision of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Dhwani BatraDivision of Scientific Resources, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Mili ShethDivision of Scientific Resources, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Martin SteinauDivision of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Jean JasinskiAgilent Technologies, Inc., Santa Clara, California, USA.
Jennifer JonesAgilent Technologies, Inc., Santa Clara, California, USA.
Mangalathu S RajeevanDivision of High-Consequence Pathogens & Pathology, Centers for Disease Control and Prevention, Atlanta, Georgia, USA mor4@cdc.gov.
Centers for Disease Control and Prevention · USAgilent Technologies (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We designed a universal human papillomavirus (HPV) typing assay based on target enrichment and whole-genome sequencing (eWGS). The RNA bait included 23,941 probes targeting 191 HPV types and 12 probes targeting beta-globin as a control. We used the Agilent SureSelect XT2 protocol for library preparation, Illumina HiSeq 2500 for sequencing, and CLC Genomics Workbench for sequence analysis. Mapping stringency for type assignment was determined based on 8 (6 HPV-positive and 2 HPV-negative) control samples. Using the optimal mapping conditions, types were assigned to 24 blinded samples. eWGS results were 100% concordant with Linear Array (LA) genotyping results for 9 plasmid samples and fully or partially concordant for 9 of the 15 cervical-vaginal samples, with 95.83% overall type-specific concordance for LA genotyping. eWGS identified 7 HPV types not included in the LA genotyping. Since this method does not involve degenerate primers targeting HPV genomic regions, PCR bias in genotype detection is minimized. With further refinements aimed at reducing cost and increasing throughput, this first application of eWGS for universal HPV typing could be a useful method to elucidate HPV epidemiology.

Indexed as

GenotypeGenome, ViralGenomicsGenotyping TechniquesHumansPapillomaviridaePapillomavirus InfectionsSequence Analysis, DNAbroad-spectrum assayHPV typingtarget enrichmentwhole-genome sequencing

Identifiers

PMID27974548
PMCPMC5328449
OpenAlexW2570269002

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.