نتایج جستجو برای: 16s rrna sequences

تعداد نتایج: 239812  

2014
Hiroshi Mori Fumito Maruyama Hiromi Kato Atsushi Toyoda Ayumi Dozono Yoshiyuki Ohtsubo Yuji Nagata Asao Fujiyama Masataka Tsuda Ken Kurokawa

The deep sequencing of 16S rRNA genes amplified by universal primers has revolutionized our understanding of microbial communities by allowing the characterization of the diversity of the uncultured majority. However, some universal primers also amplify eukaryotic rRNA genes, leading to a decrease in the efficiency of sequencing of prokaryotic 16S rRNA genes with possible mischaracterization of...

2015
Mona Mamoun Khalid A. Enan Abdelmounem E. Abdo Mohamed A. Hassan

H. pylori are a ubiquitous microorganism infecting up to half of the world’s population. A total of 81 gastric biopsies taken from patients complaining of gastric disorders in Khartoum state, Sudan screened for H.pylori. Eighteen samples (22.2%) yielded positive culture results. The majority of them were males. Also results indicated higher prevalence of H. pylori in patients with gastritis. Fu...

2014
Kanako Tago Hideomi Itoh Yoshitomo Kikuchi Tomoyuki Hori Yuya Sato Atsushi Nagayama Takashi Okubo Ronald Navarro Tomo Aoyagi Kentaro Hayashi Masahito Hayatsu

The diversity and abundance of Burkholderia species in sugarcane field soils were investigated by a 16S rRNA gene-based approach using genus-specific primers. A total of 365,721 sequences generated by the Illumina MiSeq platform were assigned to the genus Burkholderia. Nearly 58% of these sequences were placed in a previously defined cluster, including stinkbug symbionts. Quantitative PCR analy...

2017
Dieter M. Tourlousse Satowa Yoshiike Akiko Ohashi Satoko Matsukura Naohiro Noda Yuji Sekiguchi

High-throughput sequencing of 16S rRNA gene amplicons (16S-seq) has become a widely deployed method for profiling complex microbial communities but technical pitfalls related to data reliability and quantification remain to be fully addressed. In this work, we have developed and implemented a set of synthetic 16S rRNA genes to serve as universal spike-in standards for 16S-seq experiments. The s...

Journal: :Applied and environmental microbiology 1992
F J van Kuppeveld J T van der Logt A F Angulo M J van Zoest W G Quint H G Niesters J M Galama W J Melchers

Systematic computer alignment of mycoplasmal 16S rRNA sequences allowed the identification of variable regions with both genus- and species-specific sequences. Species-specific sequences of Mycoplasma collis were elucidated by asymmetric amplification and dideoxynucleotide sequencing of variable regions, using primers complementary to conserved regions of 16S rRNA. Primers selected for Mycoplas...

2012
Floyd E. Dewhirst Erin A. Klein Emily C. Thompson Jessica M. Blanton Tsute Chen Lisa Milella Catherine M. F. Buckley Ian J. Davis Marie-Lousie Bennett Zoe V. Marshall-Jones

Determining the bacterial composition of the canine oral microbiome is of interest for two primary reasons. First, while the human oral microbiome has been well studied using molecular techniques, the oral microbiomes of other mammals have not been studied in equal depth using culture independent methods. This study allows a comparison of the number of bacterial taxa, based on 16S rRNA-gene seq...

Journal: :Applied and environmental microbiology 2007
Qiong Wang George M Garrity James M Tiedje James R Cole

The Ribosomal Database Project (RDP) Classifier, a naïve Bayesian classifier, can rapidly and accurately classify bacterial 16S rRNA sequences into the new higher-order taxonomy proposed in Bergey's Taxonomic Outline of the Prokaryotes (2nd ed., release 5.0, Springer-Verlag, New York, NY, 2004). It provides taxonomic assignments from domain to genus, with confidence estimates for each assignmen...

2012
David Cleland Peter N. Green Yoko Katayama Yoshihito Uchino J. Colin Murrell Donovan P. Kelly Colin Murrell

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پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علوم و فنون دریایی خرمشهر - دانشکده علوم دریایی و اقیانوسی (شعبه خرمشهر) 1391

به منظور مطالعه فیلوژنتیکی میگوهای خانواده penaeidae سواحل بحرکان، از روش تعیین توالی ژن 16s rrna استفاده شد. استخراج dna از عضله پای شنای میگوها با روش ctab انجام شد. قطعه ژنی 16srrna با استفاده از آغازگرهای جهانی 16sar/16sbr تکثیر گردید. گرچه بعد از نمونه برداری میگوی metapenaeus sp. به عنوان گونه m. affinis، شناسایی و جداسازی شد ولی blast نتایج حاصل از تعیین توالی ژن 16s rrna نشان داد که توا...

Journal: :Journal of clinical microbiology 1992
R T Marconi L Lubke W Hauglum C F Garon

Examination of a number of previously published aligned Borrelia 16S rRNA sequences revealed the presence of regions which could serve as oligonucleotide probe targets for both species-specific identification of Borrelia burgdorferi and distinction between genomic groups. Total cellular RNA isolated from Borrelia cultures was used in slot blot analysis. Radiolabeled oligonucleotides designed to...

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