Evidence map›Paper›PMID 18445516›Full record

ArticleGenomics2008

Large-insert genome analysis technology detects structural variation in Pseudomonas aeruginosa clinical strains from cystic fibrosis patients.

Hillary S Hayden, Will Gillett, Channakhone Saenphimmachak, Regina Lim, Yang Zhou, Michael A Jacobs, Jean Chang, Laurence Rohmer, David A D'Argenio, Anthony Palmieri and 8 more

Abstract read
In one paragraph

Article in Genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Genetic Characteristics of Novel IncInfection and drug resistance · 2024
    Article
  3. Whole Genome Sequencing: Applications in Clinical Bacteriology.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Strain-dependent diversity in the Pseudomonas aeruginosa quorum-sensing regulon.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The accessory genome of Pseudomonas aeruginosa.Microbiology and molecular biology reviews : MMBR · 2010
    Review
  17. Article
  18. Article
  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

18 authors.

Hillary S HaydenGenome Center, University of Washington, Seattle, WA 98195, USA. hhayden@u.washington.edu
Will Gillett
Channakhone Saenphimmachak
Regina Lim
Yang Zhou
Michael A Jacobs
Jean Chang
Laurence Rohmer
David A D'Argenio
Anthony Palmieri
Ruth Levy
Eric Haugen
Gane K S Wong
Mitch J Brittnacher
Jane L Burns
Samuel I Miller
Maynard V Olson
Rajinder Kaul

Funding

Variation in Human Innate ImmunityU54AI057141 · NIAID · UNIVERSITY OF WASHINGTON · PI MILLER, SAMUEL I · 2003 to 2013
$102.3M
P. aeruginosa as a surrogate marker of cystic fibrosisR01DK064954 · NIDDK · UNIVERSITY OF WASHINGTON · PI MILLER, SAMUEL I. · 2004 to 2006
$2.1M
NIAID NIH HHS 5 U54 AI 057141NIAID NIH HHS U54 AI057141NIDDK NIH HHS R01 DK064954
6 · The paper itself

Abstract

Large-insert genome analysis (LIGAN) is a broadly applicable, high-throughput technology designed to characterize genome-scale structural variation. Fosmid paired-end sequences and DNA fingerprints from a query genome are compared to a reference sequence using the Genomic Variation Analysis (GenVal) suite of software tools to pinpoint locations of insertions, deletions, and rearrangements. Fosmids spanning regions that contain new structural variants can then be sequenced. Clonal pairs of Pseudomonas aeruginosa isolates from four cystic fibrosis patients were used to validate the LIGAN technology. Approximately 1.5 Mb of inserted sequences were identified, including 743 kb containing 615 ORFs that are absent from published P. aeruginosa genomes. Six rearrangement breakpoints and 220 kb of deleted sequences were also identified. Our study expands the "genome universe" of P. aeruginosa and validates a technology that complements emerging, short-read sequencing methods that are better suited to characterizing single-nucleotide polymorphisms than structural variation.

Indexed as

Genome, BacterialBase SequenceCystic FibrosisDNA FingerprintingDNA Mutational AnalysisGenetic VariationHumansMolecular Sequence DataMutagenesis, InsertionalPseudomonas aeruginosaRecombination, GeneticSequence Deletion

Identifiers

PMID18445516
PMCPMC2587363

What OpenQuestion holds

Textmetadata
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.