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Comparison of the 454 GS FLX versus 454 Titanium sequencing methods and the effect of 16S rRNA gene region MDV3100 sequenced 454/Roche recently introduced Titanium chemistry, which results in longer sequence reads than the GS FLX method (~450 nt versus ~260 nt). We thus wished to compare the results of taxonomic assignments for the same samples using the two methods. Two of the DNA specimens analyzed above were resequenced using the Titanium chemistry and results compared by compiling GSK1120212 molecular weight the proportions of all taxa (Figure 5A-C). Figure 5 Analysis of community composition

determined using different recovery and sequencing strategies. A) Results of analysis of Subjects 3 and 7 are shown comparing sequencing using 454/Roche GS FLX versus

Titanium, and use of different variable region primers. To characterize the Titanium sequencing method, 295,946 454 Titanium sequence reads were used (Additional File 2). The 454 GS FXL reads are from the samples in Additional File 1. The percentages of different bacterial families are compared in bar graphs. “”Seq. Method”" indicates GS FLX (“”X”") or Titanium (“”T”"). The families present are indicated in the key beside the graphs. “”Var. Region”" indicates the 16S rRNA gene region amplified Capmatinib nmr by each primer set (sequences used are in Additional File 4). The * indicates slightly different versions of the primers used as specified in Additional File 4. B) Percentages of sequences assigned for each primer set as a function of taxonomic level. C) Summary of regions amplified and regions sequenced for each primer set. Gray indicates the regions amplified, dark gray indicates the regions sequenced, light gray indicates regions amplified but not sequenced. Analysis of longer 16S rRNA gene region

also necessitated use of different primer Edoxaban pairs to amplify longer segments of the 16S rRNA gene. Several regions of the bacterial 16S rRNA gene are highly conserved, and multiple different primer sets have been used in published studies [4, 16–18, 37]. Previous literature has shown that 16S PCR amplification can be biased [24], so we sought to analyze this point in the context of 454/Roche pyrosequencing. To analyze the importance of primer choice for 454 Titanium pyrosequencing, we compared six primer sets, which amplified the 16S gene variable regions V1-3, V3-5, and V6-9. For each primer pair, two slightly different sequences were used. All reads were from right to left as drawn in Figure 5C, with dark gray indicating the region of sequence determination. A total of 295,946 sequence reads were used to characterize the different primers (Additional File 2). The GS FLX primers used for comparison amplified the V1-V2 region. Primer sequences are compiled in Additional File 3.

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