Evidence map›Paper›PMID 30923677›Full record

ArticleBiomolecular detection and quantification2019

Next-generation sequencing of HIV-1 single genome amplicons.

Gustavo H Kijak, Eric Sanders-Buell, Phuc Pham, Elizabeth A Harbolick, Celina Oropeza, Anne Marie O'Sullivan, Meera Bose, Charmagne G Beckett, Mark Milazzo, Merlin L Robb and 7 more

Abstract read
In one paragraph

Article in Biomolecular detection and quantification, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
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  5. Review
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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

17 authors.

Gustavo H KijakU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Eric Sanders-BuellU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Phuc PhamU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Elizabeth A HarbolickU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Celina OropezaU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Anne Marie O'SullivanU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Meera BoseU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Charmagne G BeckettNavy Bloodborne Infection Management Center, Bethesda, MD, United States.
Mark MilazzoU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Merlin L RobbU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Sheila A PeelU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Paul T ScottU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Nelson L MichaelU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Adam W ArmstrongNavy Medical Research Unit 6, Lima, Peru.
Jerome H KimU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
David M Brett-MajorDepartment of Preventive Medicine and Biostatistics, F. Edward Hébert School of Medicine, Uniformed Services University, Bethesda, MD, United States.
Sodsai TovanabutraU.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The analysis of HIV-1 sequences has helped understand the viral molecular epidemiology, monitor the development of antiretroviral drug resistance, and design candidate vaccines. The introduction of single genome amplification (SGA) has been a major advancement in the field, allowing for the characterization of multiple sequences per patient while preserving linkage among polymorphisms in the same viral genome copy. Sequencing of SGA amplicons is performed by capillary Sanger sequencing, which presents low throughput, requires a high amount of template, and is highly sensitive to template/primer mismatching. In order to meet the increasing demand for HIV-1 SGA amplicon sequencing, we have developed a platform based on benchtop next-generation sequencing (NGS) (IonTorrent) accompanied by a bioinformatics pipeline capable of running on computer resources commonly available at research laboratories. During assay validation, the NGS-based sequencing of 10 HIV-1

Indexed as

BioinformaticsHIV-1IonTorrentNext-generation sequencingSingle genome amplification

Identifiers

PMID30923677
PMCPMC6423504

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.