Evidence map›Paper›PMID 16773396›Full record

ReviewFunctional & integrative genomics2006

Ten years of bacterial genome sequencing: comparative-genomics-based discoveries.

Tim T Binnewies, Yair Motro, Peter F Hallin, Ole Lund, David Dunn, Tom La, David J Hampson, Matthew Bellgard, Trudy M Wassenaar, David W Ussery

Abstract readComparative StudyHistorical ArticleReview
PubMed Publisher
In one paragraph

Review in Functional & integrative genomics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing 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

60 citing papers in PubMed.

  1. Article
  2. Review
  3. Comparative metagenomics using pan-metagenomic graphs.bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. A phylogenetic approach to comparative genomics.Nature reviews. Genetics · 2025
    Review
  7. Review
  8. The Prevalence ofMicroorganisms · 2022
    Review
  9. Article
  10. Review
  11. Genomic comparison of Clostridium chauvoei isolates from classical and visceral clinical manifestation.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2020
    Article
  12. Article
  13. Article
  14. Inhibition of Protein Secretion inAntimicrobial agents and chemotherapy · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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.

Tim T BinnewiesCenter for Biological Sequence Analysis, Technical University of Denmark, 2800, Lyngby, Denmark.
Yair Motro
Peter F Hallin
Ole Lund
David Dunn
Tom La
David J Hampson
Matthew Bellgard
Trudy M Wassenaar
David W Ussery

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been more than 10 years since the first bacterial genome sequence was published. Hundreds of bacterial genome sequences are now available for comparative genomics, and searching a given protein against more than a thousand genomes will soon be possible. The subject of this review will address a relatively straightforward question: "What have we learned from this vast amount of new genomic data?" Perhaps one of the most important lessons has been that genetic diversity, at the level of large-scale variation amongst even genomes of the same species, is far greater than was thought. The classical textbook view of evolution relying on the relatively slow accumulation of mutational events at the level of individual bases scattered throughout the genome has changed. One of the most obvious conclusions from examining the sequences from several hundred bacterial genomes is the enormous amount of diversity--even in different genomes from the same bacterial species. This diversity is generated by a variety of mechanisms, including mobile genetic elements and bacteriophages. An examination of the 20 Escherichia coli genomes sequenced so far dramatically illustrates this, with the genome size ranging from 4.6 to 5.5 Mbp; much of the variation appears to be of phage origin. This review also addresses mobile genetic elements, including pathogenicity islands and the structure of transposable elements. There are at least 20 different methods available to compare bacterial genomes. Metagenomics offers the chance to study genomic sequences found in ecosystems, including genomes of species that are difficult to culture. It has become clear that a genome sequence represents more than just a collection of gene sequences for an organism and that information concerning the environment and growth conditions for the organism are important for interpretation of the genomic data. The newly proposed Minimal Information about a Genome Sequence standard has been developed to obtain this information.

Indexed as

Genome, BacterialBacterial VaccinesComputer SimulationDatabases, Nucleic AcidGenetic CodeGenetic VariationGenomic IslandsGenomicsHistory, 20th CenturyIntellectual PropertyInterspersed Repetitive SequencesModels, GeneticPhylogenyProteomeSequence Analysis, DNABacterial VaccinesProteome

Identifiers

What OpenQuestion holds

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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.