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In all cases, we utilized both proposed approaches to examine multicomponent InChI identifiers, i.e., the method that requires the same lists of components in the InChI identifiers being compared (denoted X⇔Y) and the method permitting the omission of some components (denoted X↔Y).
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Then, two model Rh/γ-Al2O3 catalysts, in which Rh center interacts with one oxygen or two oxygen atoms of the (100) surface of γ-Al2O3, have been compared and denoted as Rh/Al8O26H27 and Rh/Al8O26H26, respectively.
Next, we prove that the number of time slots needed in the second interval is negligible compared to, denoted by where is a small positive quantity that goes to zero as goes to infinity.
The second form is to use the phrase, "is to", between the things you are comparing, to denote that they are a ratio.
Differences in protein profiles between compared groups were denoted statistically significant if they concordantly revealed P values < 0.01 in different cohorts and blood preparation types, without multiple testing correction.
Fig. 1 demonstrates that DEM treatment reduced significantly the nuc/cyt ratio for NLS-mCherry (compare DMSO, denoted D, for ethanol-treated controls with DMSO for DEM-stressed cells).
Note: Data presented as mean ± SD; * denotes significance compared to baseline; # denotes significance compared to 6 months; P-value significant at <0.05.
* denotes p < 0.05 compared to colitis control; # denotes p < 0.05 compared to OFI + DSM 15159; § denotes p < 0.05 compared to OFI.
To compare the centroids denoted by the groups, a Manova (multivariate analysis of variance) was performed on the variables.
We compare our method, denoted as PhyCMAP, with four state-of-the-art methods: CMAPpro (Di Lena et al., 2012), NNcon (Tegge et al., 2009), PSICOV (Jones et al., 2012) and Evfold (Morcos et al., 2011).
The pre-publication history for this paper can be accessed here: * denotes p < 0.05 compared to colitis control, # denotes p < 0.05 compared to OFI + DSM 15158 group, OFI = Oligofructose and Inulin.
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