Evidence map›Paper›PMID 28811656›Full record

ArticleScientific reports2017

PhageTerm: a tool for fast and accurate determination of phage termini and packaging mechanism using next-generation sequencing data.

Julian R Garneau, Florence Depardieu, Louis-Charles Fortier, David Bikard, Marc Monot

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 510 papers.

0numbers the graph read from it
0cells of the map it votes in
510citing 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

510 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Genome sequences of sixMicrobiology resource announcements · 2026
    Article
  7. Article
  8. Article
  9. Viruses · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Genome sequence of theMicrobiology resource announcements · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Genome sequences of 19Microbiology resource announcements · 2026
    Article
  19. Complete genome sequence of theMicrobiology resource announcements · 2026
    Article
  20. Complete genome sequence ofMicrobiology resource announcements · 2026
    Article

450 more citing papers are in PubMed but not listed here.

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

5 authors.

Julian R GarneauDépartement de Microbiologie, Institut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Paris, France.ORCID 0000-0003-4579-8776
Florence DepardieuDépartement de Microbiologie, Institut Pasteur, Groupe Biologie de Synthèse, Paris, France.
Louis-Charles FortierDépartement de Microbiologie et d'infectiologie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, QC, Canada.
David BikardDépartement de Microbiologie, Institut Pasteur, Groupe Biologie de Synthèse, Paris, France. david.bikard@pasteur.fr.ORCID 0000-0002-5729-1211
Marc MonotDépartement de Microbiologie, Institut Pasteur, Laboratoire Pathogenèse des bactéries anaérobies, Paris, France. marc.monot@pasteur.fr.ORCID 0000-0003-0738-7335

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The worrying rise of antibiotic resistance in pathogenic bacteria is leading to a renewed interest in bacteriophages as a treatment option. Novel sequencing technologies enable description of an increasing number of phage genomes, a critical piece of information to understand their life cycle, phage-host interactions, and evolution. In this work, we demonstrate how it is possible to recover more information from sequencing data than just the phage genome. We developed a theoretical and statistical framework to determine DNA termini and phage packaging mechanisms using NGS data. Our method relies on the detection of biases in the number of reads, which are observable at natural DNA termini compared with the rest of the phage genome. We implemented our method with the creation of the software PhageTerm and validated it using a set of phages with well-established packaging mechanisms representative of the termini diversity, i.e. 5'cos (Lambda), 3'cos (HK97), pac (P1), headful without a pac site (T4), DTR (T7) and host fragment (Mu). In addition, we determined the termini of nine Clostridium difficile phages and six phages whose sequences were retrieved from the Sequence Read Archive. PhageTerm is freely available (https://sourceforge.net/projects/phageterm), as a Galaxy ToolShed and on a Galaxy-based server (https://galaxy.pasteur.fr).

Indexed as

Genome, ViralVirus AssemblyAnimalsBacteriophagesClostridioides difficileDNA, ViralDNA, Viral

Identifiers

PMID28811656
PMCPMC5557969

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.