Radial distribution function and coordination number analyses are further performed to reveal the underlying atomistic origins of the removal rate anisotropy.
Note that previously performed frequency-wave number analyses have ensured that the westward migrating component is the dominant 8-h oscillation of 8-h ES (not shown here), agreeing with the results presented by Moudden and Forbes (2013).
The chemical explosive mode and Damköhler number analyses verify that for the baseline and uncorrelated T ϕ cases, the deflagration mode is predominant at the reaction fronts for large T′ and/or ϕ′.
The budget and Damköhler number analyses verify that although a mixed combustion mode of deflagration and spontaneous ignition exists during the early phase of the DDFS combustion, the spontaneous ignition becomes predominant during the main combustion, and hence, the spread-out of heat release rate in the DDFS combustion is mainly governed by the direct injection process of i-C8H18.
Chemical explosive mode (CEM), displacement speed, and Damköhler number analyses revealed that the high degree of thermal stratification induces deflagration rather than spontaneous ignition at the reaction fronts, rendering the mean heat release rate more distributed over time subsequent to thermal runaway occurring at the highest temperature regions in the domain.
Displacement speed and Damköhler number analyses reveal that the high degree of thermal stratification induces deflagration rather than spontaneous ignition at the reaction fronts, and hence, the mean heat release rate is smoother subsequent to thermal runaway occurring at the highest temperature regions in the domain.
The copy number analyses (Fig. 1E) demonstrated that all variant types were present in similar copy numbers and that the total copy number of the rDNA pool analyzed by this method was between 49 to 82, in agreement with the Stu I- and Sty I-RFLP copy number analyses (Fig. 1A).
Briefly, we used LINE-1 gene, which is the most abundant autonomous retrotransposon in the human consisting of 17% of the genome [34], as a reference gene for all copy number analyses.
Our initial copy number analyses revealed complex chromosomal rearrangements with approximately 96 large regions of chromosome copy number differences in the 468LN versus the 468GFP cells, ranging up to 100 megabases (Figure 2).
We found a large variability in amplification bias among the amplified products obtained by multiple displacement amplification (MDA), and this bias had a severe effect on the genotype and chromosomal copy number analyses.
