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. Author manuscript; available in PMC: 2018 Feb 5.
Published in final edited form as: Clin Microbiol Infect. 2016 Jan 22;22(5):464–465. doi: 10.1016/j.cmi.2016.01.013

Figure 1.

Figure 1

Inter-individual variation, rather than celecoxib administration, accounts for most microbiome diversity within a longitudinal human cohort. A) Average bacterial richness (as observed operational taxonomic units, OTUs) in subjects’ stools during run-in (before), after 10 days of celecoxib administration, and 7–14 days after completing drug administration (follow-up). B) Unweighted UniFrac PCoA comparing microbiome similarity between samples. Each sample is represented by a point, color-coded by subject. Note that samples predominantly cluster by subject, indicating no consistent effect of celecoxib treatment on bacterial composition.