7 research outputs found

    Caries Phenotype Determination.

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    <p>Quantitative Light fluorescence (QLF) of occlusal surfaces of C-F and C-A subjects. <u>Quantitative light fluorescence </u>(QLF) examination was conducted to complement clinical examinations and the DIFOTI procedure. C-A subjects had an average of 12 (range = 6–17) decayed tooth surfaces whereas C-F subjects presented with a decay component = 0. Subjects had an average of 11.5 decayed surfaces and 2.3 restored surfaces. These individuals presented with primary dentition only. C-A subjects had an average of 74 healthy surfaces.</p

    Comparison of C-F and C-A Species Abundance.

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    <p>The 16 most abundant species and their relative abundance in C-F and C-A subject pools.</p

    Differential Representation of Genera in the C-F and C-A Microbiomes.

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    <p>Bars to the left correspond to over-representation of genera in the C-F subject pool, and bars to the right correspond to over-representation in the C-A subject pool. Bar color key references percentage of the total 16S sequences.</p

    Statistical Significance of Differential Species Abundance Between the C-F and C-A Microbiomes.

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    <p>Volcano plot depicting the relationship between –log p-values resulting from standard binomial tests of frequency differences between C-A and C-F for each phylotype identified as a function of the standardized difference in phylotype frequency between C-A and C-F.</p

    Phylogeny of Carbapenemase-producing Klebsiella and Carbapenemase-producing Acinetobacter.

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    <p>A-C represent the same <i>Klebsiella</i> isolates from the same outbreak event, and Fig 2D–2F represent the same <i>Acinetobacter</i> isolates from a separate same outbreak event. However, depending on the clustering method and software program used, different results can be obtained. This highlights the need for standardized approaches.</p
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