Evidence map›Paper›PMID 33562285›Full record

ArticleViruses2021

Deep Impact of Random Amplification and Library Construction Methods on Viral Metagenomics Results.

Béatrice Regnault, Thomas Bigot, Laurence Ma, Philippe Pérot, Sarah Temmam, Marc Eloit

Registry-linked trialOpen access · goldAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Viruses, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05388968 (Pathogen Detection by Metatranscriptomic Next Generation Sequencing in the Trophoblast Collected in Women Carrying a Fetus With Increasing Nuchal Translucency in the First Trimester of Pregnancy), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.5field-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.

NCT05388968 completednot on this mapstarted 2022, after this paper: background citation

Pathogen Detection by Metatranscriptomic Next Generation Sequencing in the Trophoblast Collected in Women Carrying a Fetus With Increasing Nuchal Translucency in the First Trimester of Pregnancy

TypeobservationalSponsorAssistance Publique - Hôpitaux de ParisRan2022 to 2025Enrolled78ConditionsIncreased Nuchal Translucency in the First Trimester of PregnancyArmsMetatranscriptomic, Specific microbiologic diagnosis
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Wastewater Metavirome Diversity: Exploring Replicate Inconsistencies and Bioinformatic Tool Disparities.International journal of environmental research and public health · 2025
    Article
  5. Broad range molecular detection methods identify onlyOne health (Amsterdam, Netherlands) · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
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  15. Review
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

6 authors at 1 institution in 1 country.

Béatrice RegnaultPathogen Discovery Laboratory, Institut Pasteur, 75015 Paris, France.
Thomas BigotBioinformatics and Biostatistics Hub, Computational Biology Department, Institut Pasteur, 75015 Paris, France.ORCID 0000-0001-8504-4675
Laurence MaBiomics Platform, C2RT, Institut Pasteur, 75015 Paris, France.
Philippe PérotPathogen Discovery Laboratory, Institut Pasteur, 75015 Paris, France.
Sarah TemmamPathogen Discovery Laboratory, Institut Pasteur, 75015 Paris, France.ORCID 0000-0003-3655-9220
Marc EloitPathogen Discovery Laboratory, Institut Pasteur, 75015 Paris, France.ORCID 0000-0002-1853-7207
Institut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clinical metagenomics is a broad-range agnostic detection method of pathogens, including novel microorganisms. A major limit is the low pathogen load compared to the high background of host nucleic acids. To overcome this issue, several solutions exist, such as applying a very high depth of sequencing, or performing a relative enrichment of viral genomes associated with capsids. At the end, the quantity of total nucleic acids is often below the concentrations recommended by the manufacturers of library kits, which necessitates to random amplify nucleic acids. Using a pool of 26 viruses representative of viral diversity, we observed a deep impact of the nature of sample (total nucleic acids versus RNA only), the reverse transcription, the random amplification and library construction method on virus recovery. We further optimized the two most promising methods and assessed their performance with fully characterized reference virus stocks. Good genome coverage and limit of detection lower than 100 or 1000 genome copies per mL of plasma, depending on the genome viral type, were obtained from a three million reads dataset. Our study reveals that optimized random amplification is a technique of choice when insufficient amounts of nucleic acid are available for direct libraries constructions.

Indexed as

Genome, ViralGenomic LibraryHumansLimit of DetectionMetagenomicsNucleic Acid Amplification TechniquesVirusesrandom amplificationsensitivityviral metagenomics

Identifiers

PMID33562285
PMCPMC7915491
OpenAlexW3127392154

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.