article Open AccessTop 10% cited
Design and Evaluation of Useful Bacterium-Specific PCR Primers That Amplify Genes Coding for Bacterial 16S rRNA
Applied and Environmental Microbiology · 1998 · Vol. 64(2) · pp. 795–799
Julian R. Marchesi✉(University of Wales)Takuichi Sato(Niigata University)Andrew J. Weightman(University of Wales)Tracey A. Martin(University of Wales)John C. Fry(University of Wales)Sarah Hiom(University Of Bristol Dental Hospital)William G. Wade(Guy's Hospital)
Abstract
We report the design and evaluation of PCR primers 63f and 1387r for amplification of 16S rRNA genes from bacteria. Their specificity and efficacy were tested systematically with a bacterial species and environmental samples. They were found to be more useful for 16S rRNA gene amplification in ecological and systematic studies than PCR amplimers that are currently more generally used.
Molecular Biology Techniques and ApplicationsBacteriophages and microbial interactionsGenomics and Phylogenetic StudiesBiology16S ribosomal RNAGeneBacteriaGeneticsPolymerase chain reactionComputational biologyRibosomal RNABacterial geneticsMicrobiology
MeSH terms
BacteriaBase SequenceDNA, RibosomalMolecular Sequence DataRNA, Ribosomal, 16SPolymerase Chain ReactionDNA Primers
Funding
- Natural Environment Research Council
Citations
1,810
FWCI
5.28
field-weighted impact
References
17
Percentile
96%
vs. same field & year
Citations per year
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References
16S/23S rRNA sequencing
Medical Entomology and Zoology · 1991 · 7,957 citations
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