Figure 1.
The low frequency of single-nucleotide variants (SNVs) of a recently published CMAG. A randomly chosen region, centered on position 123,456 (1100 bp in length) of the CMAG of Candidatus Fluviicola riflensis is shown with mapped reads (Banfield et al. 2017). SNVs that only occur once are indicated by black boxes, and the one replicated SNV is indicated by a red box. Clearly, the consensus sequence is well supported. The mapping of reads to the genome was performed by Bowtie 2 and visualized via Geneious.
