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Borjigin argues that the rat data are compelling enough to drive further study of near-death experiences in humans.
The rat data are an exception; hardly any values larger than 0.6 were observed.
Finally, the rabbit and rat data are briefly discussed in the context of the available epidemiological data for glyphosate.
The rat data are single-ended sequencing data, while the mouse data are paired-end sequencing data.
Additionally, the empirical mouse and rat data are represented as horizontal lines in their respective plots, at average sequencing depths of 10,000 to 100,000 ×.
The rat data are of questionable relevance to human infants, given the variety of cross-species differences in the ontogeny of toxicokinetic systems (Ginsberg et al. 2004).
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The residence times derived from the rat data were integrated as the area under the time-activity curve.
First the rat data were analyzed using an ICA dividing the rat rsfMRI signal into 40 components, comparable with an earlier study applying ICA for rat data [14].
Our database consisting of Wistar rat data was used to generate an SVM.
Grip strength did not correlate with serum cytokine levels when both aged and young rat data was combined due to the large number of young rats with no increase in serum cytokines (data not shown).
Most of the rat data was derived from one animal per litter and was thus analyzed using either Student's t-test or one-way analysis of variance (ANOVA) followed by the Bonferroni post hoc test; for experiments in which several animals were used per litter (mRNA expression analysis), we accounted for within-litter effects using two-factor ANOVA.
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