Evidence map›Paper›PMID 29940028›Full record

ArticlePloS one2018

An optimized methodology for whole genome sequencing of RNA respiratory viruses from nasopharyngeal aspirates.

Stephanie Goya, Laura E Valinotto, Estefania Tittarelli, Gabriel L Rojo, Mercedes S Nabaes Jodar, Alexander L Greninger, Jonathan J Zaiat, Marcelo A Marti, Alicia S Mistchenko, Mariana Viegas

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 34 citations in OpenAlex.

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  5. Genomic characterisation of respiratory syncytial virus: a novel system for whole genome sequencing and full-length G and F gene sequences.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2023
    Article
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  8. Agnostic Sequencing for Detection of Viral Pathogens.Clinical microbiology reviews · 2023
    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

10 authors at 5 institutions in 2 countries.

Stephanie GoyaRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.ORCID 0000-0001-7479-3064
Laura E ValinottoRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Estefania TittarelliRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Gabriel L RojoRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Mercedes S Nabaes JodarRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Alexander L GreningerDepartment of Laboratory Medicine, University of Washington, Seattle, Washington, United States of America.
Jonathan J ZaiatConsejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Buenos Aires, Argentina.
Marcelo A MartiConsejo Nacional de Investigaciones Científicas y Tecnológicas (CONICET), Buenos Aires, Argentina.
Alicia S MistchenkoRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Mariana ViegasRicardo Gutiérrez Children's Hospital, Ciudad Autónoma Buenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARComisión de Investigaciones Científicas · ARHospital General de Niños Ricardo Gutierrez · ARMinisterio de Salud · ARUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Over the last decade, the number of viral genome sequences deposited in available databases has grown exponentially. However, sequencing methodology vary widely and many published works have relied on viral enrichment by viral culture or nucleic acid amplification with specific primers rather than through unbiased techniques such as metagenomics. The genome of RNA viruses is highly variable and these enrichment methodologies may be difficult to achieve or may bias the results. In order to obtain genomic sequences of human respiratory syncytial virus (HRSV) from positive nasopharyngeal aspirates diverse methodologies were evaluated and compared. A total of 29 nearly complete and complete viral genomes were obtained. The best performance was achieved with a DNase I treatment to the RNA directly extracted from the nasopharyngeal aspirate (NPA), sequence-independent single-primer amplification (SISPA) and library preparation performed with Nextera XT DNA Library Prep Kit with manual normalization. An average of 633,789 and 1,674,845 filtered reads per library were obtained with MiSeq and NextSeq 500 platforms, respectively. The higher output of NextSeq 500 was accompanied by the increasing of duplicated reads percentage generated during SISPA (from an average of 1.5% duplicated viral reads in MiSeq to an average of 74% in NextSeq 500). HRSV genome recovery was not affected by the presence or absence of duplicated reads but the computational demand during the analysis was increased. Considering that only samples with viral load ≥ E+06 copies/ml NPA were tested, no correlation between sample viral loads and number of total filtered reads was observed, nor with the mapped viral reads. The HRSV genomes showed a mean coverage of 98.46% with the best methodology. In addition, genomes of human metapneumovirus (HMPV), human rhinovirus (HRV) and human parainfluenza virus types 1-3 (HPIV1-3) were also obtained with the selected optimal methodology.

Indexed as

Genome, ViralFemaleHigh-Throughput Nucleotide SequencingHumansLarynxMaleNasal CavityRespiratory Syncytial Viruses

Identifiers

PMID29940028
PMCPMC6016902
OpenAlexW2809814483

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.