Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

SNaPaer: a practical single nucleotide polymorphism multiplex assay for genotyping of Pseudomonas aeruginosa.

PloS one - 1 Jan 2013

Eusebio Nadia, Pinheiro Tiago, Amorim Adelina A, Gamboa Fernanda, Saraiva Lucília, Gusmão Leonor, Amorim António, Araujo Ricardo

Abstract excerpt

Multilocus sequence typing (MLST) represents the gold standard genotyping method in studies concerning microbial population structure, being particularly helpful in the detection of clonal relatedness. However, its applicability on large-scale genotyping is limited due to the high cost and time spent on the task. The selection of the most informative nucleotide positions simplifies genomic characterization of...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Bacterial Typing Techniques
Share to DNA Primers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electrophoresis, Polyacrylamide Gel

Share to Hospitals

Share to Multilocus Sequence Typing

Share to Multiplex Polymerase Chain Reaction

Share to Portugal

Share to Pseudomonas aeruginosa

Source

Open in PubMed Open full text

Identifiers

PMID: 23776608
DOI: 10.1371/journal.pone.0066083
PMCID: PMC3680407

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

SNaPaer: a practical single nucleotide polymorphism multiplex assay for genotyping of Pseudomonas aeruginosa.PMID 23776608Read ↗

Molecular identification and genotyping of Pseudomonas aeruginosa isolated from cystic fibrosis and non-cystic fibrosis patients with bronchiectasis.Semantic proximity Read ↗

Broad Genome Sequencing of Environmental and Clinical Strains and Genotyping.Semantic proximity Read ↗

Population structure of Pseudomonas aeruginosa through a MLST approach and antibiotic resistance profiling of a Mexican clinical collection.Semantic proximity Read ↗

SNaPBcen: a novel and practical tool for genotyping Burkholderia cenocepacia.Semantic proximity Read ↗

Single-Nucleotide Polymorphism-Based Genetic Diversity Analysis of Clinical Pseudomonas aeruginosa Isolates.Semantic proximity Read ↗

Genomic characterisation of an international Pseudomonas aeruginosa reference panel indicates that the two major groups draw upon distinct mobile gene pools.Semantic proximity Read ↗

Diversity and epidemiological profile of Pseudomonas aeruginosa from drinking water in Brazil genotyped using multi-locus sequence typing.Semantic proximity Read ↗

Fast and simple epidemiological typing of Pseudomonas aeruginosa using the double-locus sequence typing (DLST) method.Semantic proximity Read ↗

Antibiotic resistance and population structure of cystic fibrosis Pseudomonas aeruginosa isolates from a Spanish multi-centre study.Semantic proximity Read ↗

Genetic diversity of Pseudomonas aeruginosa isolated from clinical samples with ISSR molecular marker in a tertiary care teaching hospital.Semantic proximity Read ↗

In-Depth Study of a Nosocomial Outbreak Caused by Extensively Drug-Resistant Pseudomonas aeruginosa Using Whole Genome Sequencing Coupled With a Polymerase Chain Reaction Targeting Strain-Specific Single Nucleotide Polymorphisms.Semantic proximity Read ↗

SNaPAfu: a novel single nucleotide polymorphism multiplex assay for aspergillus fumigatus direct detection, identification and genotyping in clinical specimens.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.