Evidence map›Paper›PMID 22962364›Full record

ArticleNucleic acids research2013

Complete viral RNA genome sequencing of ultra-low copy samples by sequence-independent amplification.

Christine M Malboeuf, Xiao Yang, Patrick Charlebois, James Qu, Aaron M Berlin, Monica Casali, Kendra N Pesko, Christian L Boutwell, John P DeVincenzo, Gregory D Ebel and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 82 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. 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. Review
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  11. Contribution of Resident Memory CD8Pathogens (Basel, Switzerland) · 2019
    Review
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  13. Review
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  15. Article
  16. Article
  17. Article
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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

14 authors at 4 institutions in 1 country.

Christine M MalboeufBroad Institute of MIT and Harvard, Cambridge, MA 02142, USA. malboeuf@broadinstitute.org
Xiao Yang
Patrick Charlebois
James Qu
Aaron M Berlin
Monica Casali
Kendra N Pesko
Christian L Boutwell
John P DeVincenzo
Gregory D Ebel
Todd M Allen
Michael C Zody
Matthew R Henn
Joshua Z Levin
Broad Institute · USUniversity of New Mexico · USRagon Institute of MGH, MIT and Harvard · USUniversity of Tennessee Health Science Center · US

Funding

Recognition of HIV-1 by Innate Immunity Receptors during Primary InfectionP01AI074415 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALLEN, TODD M · 2008 to 2013
$17.3M
Biology of Infectious Diseases &InflammationT32AI007538 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Michelle A Ozbun · 1998 to 2026
$5.2M
NIAID NIH HHS HHSN272200900006CNIAID NIH HHS HHSN272200900018CNIAID NIH HHS P01-AI074415NIAID NIH HHS T32 AI007538PHS HHS HHSN27220090018C
6 · The paper itself

Abstract

RNA viruses are the causative agents for AIDS, influenza, SARS, and other serious health threats. Development of rapid and broadly applicable methods for complete viral genome sequencing is highly desirable to fully understand all aspects of these infectious agents as well as for surveillance of viral pandemic threats and emerging pathogens. However, traditional viral detection methods rely on prior sequence or antigen knowledge. In this study, we describe sequence-independent amplification for samples containing ultra-low amounts of viral RNA coupled with Illumina sequencing and de novo assembly optimized for viral genomes. With 5 million reads, we capture 96 to 100% of the viral protein coding region of HIV, respiratory syncytial and West Nile viral samples from as little as 100 copies of viral RNA. The methods presented here are scalable to large numbers of samples and capable of generating full or near full length viral genomes from clone and clinical samples with low amounts of viral RNA, without prior sequence information and in the presence of substantial host contamination.

Indexed as

Genome, ViralNucleic Acid Amplification TechniquesSequence Analysis, RNABase SequenceHIVHumansMolecular Sequence DataRespiratory Syncytial VirusesReverse Transcriptase Polymerase Chain ReactionRNA, ViralWest Nile virusRNA, Viral

Identifiers

PMID22962364
PMCPMC3592391
OpenAlexW2113252693

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.