Direct 16S rRNA-seq from bacterial communities: a PCR-independent approach to simultaneously assess microbial diversity and functional activity potential of each taxon-Reference-Cited by-同舟云学术

Direct 16S rRNA-seq from bacterial communities: a PCR-independent approach to simultaneously assess microbial diversity and functional activity potential of each taxon

Published:2016-08-31 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Rosselli Riccardo,Romoli Ottavia,Vitulo Nicola,Vezzi Alessandro,Campanaro Stefano,de Pascale Fabio,Schiavon Riccardo,Tiarca Maurizio,Poletto Fabio,Concheri Giuseppe,Valle Giorgio,Squartini Andrea

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep32165.pdf

Reference67 articles.

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3. Rzhetsky, A. Estimating substitution rates in ribosomal RNA genes. Genetics. 141, 771–783 (1995).

4. Otsuka, J., Terai, G. & Nakano, T. Phylogeny of organisms investigated by the base-pair changes in the stem regions of small and large ribosomal subunit RNAs. J. Mol. Evol. 48, 218–235 (1999).

5. Wang, H. & Hickey, D. Evidence for strong selective constraint acting on the nucleotide composition of 16S ribosomal RNA genes. Nucl. Ac. Res. 30, 2501–2507 (2002).

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