| Literature DB >> 32025980 |
Hiromasa Tanaka1, Yoshiyuki Matsuo2, So Nakagawa3, Kenichiro Nishi1,4, Akihisa Okamoto1,4, Shinichi Kai5, Teppei Iwai1, Yoshiteru Tabata1, Takeshi Tajima6, Yuji Komatsu6, Motohiko Satoh6, Kirill Kryukov3, Tadashi Imanishi3, Kiichi Hirota7.
Abstract
Entities:
Year: 2019 PMID: 32025980 PMCID: PMC6967274 DOI: 10.1186/s40981-019-0244-z
Source DB: PubMed Journal: JA Clin Rep ISSN: 2363-9024
Fig. 1Taxonomic assignment of the 16S rRNA genes in sputum samples. The samples were subjected to 16S rRNA amplicon sequencing using MinION™ (Oxford Nanopore Technologies, Oxford, UK), and the percentage of reads (with the abundance over 2%) belonging to the identified bacterial species is shown. Sequencing for 5 min generated 470,231 reads. A total of 41,136 reads were aligned with one of the bacterial 16S rRNA gene sequences, and 65.3% reads were aligned with Stenotrophomonas maltophilia and 15.7% reads were aligned with Pseudomonas aeruginosa