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Diagnostic Bacteriology

Overview of attention for book
Cover of 'Diagnostic Bacteriology'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Whole-Genome Enrichment Using RNA Probes and Sequencing of Chlamydia trachomatis Directly from Clinical Samples
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    Chapter 2 Characterization of Sinus Microbiota by 16S Sequencing from Swabs
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    Chapter 3 Molecular Subtyping of Salmonella Typhimurium with Multiplex Oligonucleotide Ligation-PCR (MOL-PCR)
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    Chapter 4 Detection of Helicobacter pylori DNA in Formalin-Fixed Paraffin-Embedded Gastric Biopsies Using Laser Microdissection and qPCR
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    Chapter 5 Mycobacterial Load Assay
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    Chapter 6 Defining Diagnostic Biomarkers Using Shotgun Proteomics and MALDI-TOF Mass Spectrometry
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    Chapter 7 Detection and Typing of “Candidatus Phytoplasma ” spp. in Host DNA Extracts Using Oligonucleotide-Coupled Fluorescent Microspheres
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    Chapter 8 Detection of Helicobacter pylori in the Gastric Mucosa by Fluorescence In Vivo Hybridization
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    Chapter 9 Rapid Antibiotic Susceptibility Testing for Urinary Tract Infections
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    Chapter 10 Detection and Differentiation of Lyme Spirochetes and Other Tick-Borne Pathogens from Blood Using Real-Time PCR with Molecular Beacons
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    Chapter 11 Methods for Real-Time PCR-Based Diagnosis of Chlamydia pneumoniae, Chlamydia psittaci, and Chlamydia abortus Infections in an Opened Molecular Diagnostic Platform
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    Chapter 12 Real-Time PCR to Identify Staphylococci and Assay for Virulence from Blood
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    Chapter 13 Multiplex Peptide Nucleic Acid Fluorescence In Situ Hybridization (PNA-FISH) for Diagnosis of Bacterial Vaginosis
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    Chapter 14 A Closed-tube Loop-Mediated Isothermal Amplification Assay for the Visual Endpoint Detection of Brucella spp. and Mycobacterium avium subsp. paratuberculosis
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    Chapter 15 Highly Specific Ligation-dependent Microarray Detection of Single Nucleotide Polymorphisms
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    Chapter 16 Multilocus Sequence Typing (MLST) for Cronobacter spp.
  18. Altmetric Badge
    Chapter 17 Diagnostic Bacteriology: Raman Spectroscopy
Attention for Chapter 2: Characterization of Sinus Microbiota by 16S Sequencing from Swabs
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (84th percentile)
  • High Attention Score compared to outputs of the same age and source (97th percentile)

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9 X users

Citations

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Chapter title
Characterization of Sinus Microbiota by 16S Sequencing from Swabs
Chapter number 2
Book title
Diagnostic Bacteriology
Published in
Methods in molecular biology, June 2017
DOI 10.1007/978-1-4939-7037-7_2
Pubmed ID
Book ISBNs
978-1-4939-7035-3, 978-1-4939-7037-7
Authors

Thad W. Vickery B.A., Jennifer M. Kofonow M.S., Vijay R. Ramakrishnan M.D., Vickery, Thad W., Kofonow, Jennifer M., Ramakrishnan, Vijay R., Thad W. Vickery, Jennifer Kofonow, Vijay R. Ramakrishnan, Jennifer M. Kofonow

Editors

Kimberly A. Bishop-Lilly

Abstract

New culture-independent microbiology methods are leading to a paradigm shift in our understanding of how the microbial community at the mucosal surface impacts sinonasal health and disease. Whereas traditional culture-based protocols were designed to identify specific pathogens in order to direct antibiotic therapies and eradicate bacteria, newer molecular techniques allow for the identification of both culturable and nonculturable bacteria in diverse communities. As a result of the recent explosion in the use of molecular techniques, we are gaining an understanding of how commensal bacteria may help modulate the host immune response and promote homeostasis. Here, we describe the general workflow of microbiome sequencing including the detailed methods for extracting mixed-community genomic DNA from sinonasal swabs, amplifying bacterial 16S rRNA genes using quantitative PCR, and preparing the samples for next-generation sequencing on the most commonly used sequencing platforms.

X Demographics

X Demographics

The data shown below were collected from the profiles of 9 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 19%
Student > Bachelor 4 15%
Student > Ph. D. Student 3 11%
Student > Master 3 11%
Student > Doctoral Student 2 7%
Other 5 19%
Unknown 5 19%
Readers by discipline Count As %
Immunology and Microbiology 6 22%
Agricultural and Biological Sciences 4 15%
Biochemistry, Genetics and Molecular Biology 3 11%
Medicine and Dentistry 3 11%
Engineering 2 7%
Other 2 7%
Unknown 7 26%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 12. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 26 September 2017.
All research outputs
#2,567,641
of 22,979,862 outputs
Outputs from Methods in molecular biology
#469
of 13,148 outputs
Outputs of similar age
#49,830
of 317,056 outputs
Outputs of similar age from Methods in molecular biology
#7
of 303 outputs
Altmetric has tracked 22,979,862 research outputs across all sources so far. Compared to these this one has done well and is in the 88th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,148 research outputs from this source. They receive a mean Attention Score of 3.4. This one has done particularly well, scoring higher than 96% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 317,056 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 84% of its contemporaries.
We're also able to compare this research output to 303 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 97% of its contemporaries.