(DOC 924 KB) Additional file 2 : Figure S2 Non-coverage rates at

(DOC 924 KB) Additional file 2 : Figure S2. Non-coverage rates at the phylum level. The figures show the non-coverage rates of different primers at the phylum level: A Primer 27F; B Primer 338F; C Primer 338R; D Primer 519F; E Protein Tyrosine Kinase inhibitor Primer 519R; F Primer 907R; G Primer 1390R; and H Primer 1492R. (DOC 214 KB) Additional file 3 : Table S1; Table S2; Table S3; Table S4; Table S5. Primer binding-site sequence variants. Frequently observed sequence

variants at different primer binding sites are listed in different tables: Table S1 Primer 27F; Table S2 Primer 338F; Table S3 Primer 338R; Table S4 Primer 519F; and Table S5 Primer 907R. (DOC 258 KB) Additional file 4 : Figure S3. Elimination of primer contamination. The figure shows the elimination of sequences that are thought to lack correct primer trimming in the Trichostatin A order RDP dataset. (DOC 463 KB) References 1. Olsen GJ, Lane DJ, Giovannoni SJ, Pace NR, Stahl DA: Microbial ecology and evolution: a ribosomal RNA approach. Annu Rev Microbiol 1986, 40:337–365.PubMedCrossRef 2. Schmidt TM, Delong EF, Pace NR: Analysis of a marine picoplankton community by 16S rRNA gene cloning and sequencing. J Bacteriol 1991, 173:4371–4378.PubMed 3. Sharkey FH, Banat IM, Marchant R: Detection and quantification of

gene expression in environmental bacteriology. Appl Environ Microb 2004, 70:3795–3806.CrossRef 4. Steffan RJ, Atlas RM: Polymerase chain reaction: applications in environmental microbiology. Annu Rev Microbiol 1991, 45:137–161.PubMedCrossRef 5.

Forney LJ, Zhou X, Brown CJ: Molecular microbial ecology: land of the one-eyed king. Curr Opin Microbiol 2004, 7:210–220.PubMedCrossRef 6. Smith S, Vigilant L, Morin PA: The effects of sequence length and oligonucleotide PLEKHB2 mismatches on 5′ exonuclease assay efficiency. Nucleic Acids Res 2002, 30:e111.PubMedCrossRef 7. von Wintzingerode F, Gobel UB, Stackebrandt E: Determination of microbial diversity in environmental samples: pitfalls of PCR-based rRNA analysis. FEMS Microbiol Rev 1997, 21:213–229.PubMedCrossRef 8. Polz MF, Cavanaugh CM: Bias in template-to-product ratios in multitemplate PCR. Appl Environ Microb 1998, 64:3724–3730. 9. Reysenbach AL, Giver LJ, Wickham GS, Pace NR: Differential amplification of rRNA genes by polymerase chain reaction. Appl Environ Microb 1992, 58:3417–3418. 10. Baker GC, Smith JJ, Cowan DA: Review and re-analysis of domain-specific 16S primers. J Microbiol Meth 2003, 55:541–555.CrossRef 11. Huws SA, Edwards JE, Kim EJ, Scollan ND: Specificity and sensitivity of eubacterial primers utilized for molecular profiling of bacteria within complex microbial ecosystems. J Microbiol Meth 2007, 70:565–569.CrossRef 12. Wang Y, Qian PY: Conservative fragments in bacterial 16S rRNA genes and primer design for 16S ribosomal DNA amplicons in metagenomic studies. PLoS One 2009, 4:e7401.PubMedCrossRef 13.

Leave a Reply

Your email address will not be published. Required fields are marked *

*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>