Evidence map›Paper›PMID 24467869›Full record

ArticleMicrobial informatics and experimentation2014

A systematic search for discriminating sites in the 16S ribosomal RNA gene.

Hilde Vinje, Trygve Almøy, Kristian Hovde Liland, Lars Snipen

Abstract read
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Article in Microbial informatics and experimentation, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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  4. Applied and environmental microbiology · 2019
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

Hilde VinjeDepartment of Chemistry, Biotechnology and Food Sciences, Norwegian University of Life Sciences, Ås N-1432, Norway. hilde.vinje@nmbu.no.
Trygve Almøy
Kristian Hovde Liland
Lars Snipen

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 16S rRNA is by far the most common genomic marker used for prokaryotic classification, and has been used extensively in metagenomic studies over recent years. Along the 16S gene there are regions with more or less variation across the kingdom of bacteria. Nine variable regions have been identified, flanked by more conserved parts of the sequence. It has been stated that the discriminatory power of the 16S marker lies in these variable regions. In the present study we wanted to examine this more closely, and used a supervised learning method to search systematically for sites that contribute to correct classification at either the phylum or genus level.

resultsWhen classifying phyla the site selection algorithm located 50 discriminative sites. These were scattered over most of the alignments and only around half of them were located in the variable regions. The selected sites did, however, have an entropy significantly larger than expected, meaning they are sites of large variation. We found that the discriminative sites typically have a large entropy compared to their closest neighbours along the alignments. When classifying genera the site selection algorithm needed around 80% of the sites in the 16S gene before the classification error reached a minimum. This means that all variation, in both variable and conserved regions, is needed in order to separate genera.

conclusionsOur findings does not support the statement that the discriminative power of the 16S gene is located only in the variable regions. Variable regions are important, but just as many discriminative sites are found in the more conserved parts. The discriminative power is typically found in sites of large variation located inside shorter regions of higher conservation.

Identifiers

PMID24467869
PMCPMC3910680

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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.