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The crystallization temperature of high-oleic acetyl-TAG (by differential scanning calorimetry at 1.0 °C/min) was reduced by 30 °C compared to control TAG.
Control tag densities are also used to assess the significance of peaks in the ChIP sample.
The distribution of all protein ratios for the androgen-treated sample (tag 115) versus control (tag 116) is shown in Supplementary Figure S1A.
Some methods implement background subtraction by calling peaks from the difference between ChIP and normalized control tag densities [15], [28], [31], while others use control data to identify and compensate large duplications or deletions in the genome [23].
Collectively, these data argue that variation in genes involved in apoptosis control TAG accumulation.
Some methods use sequence data from a control dataset and then use the control tag densities to assess the significance of peaks in the ChIP sample set.
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an enhanced ability for users to control tagging and posting on other user profiles.
These studies demonstrate that these new tags exhibit higher affinity and thus improved selectivity with both the immobilised Ni2+- and the Cu2+-tacn complexes compared to control tags, such as [His]6.
**Acronyms of the control tags are as follows: i: illumination changes, f: facial expression, o: occlusion, r: head rotation, f: frontal face, nf: near-frontal (up to 15° yaw), s: scale change, b: blur.
One straightforward approach is to calculate the fold enrichment of ChIP tags over normalized control tags in candidate regions, to account for the fluctuating background signal [16], [18], [27], [32].
None of the control TAg-injected mice showed disease by the end of the study period.
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