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Distribution of shift length categories on the individual level can be found in table 1.
To assess whether the mutations under selection during tumorigenesis occured by tumor SMAFS, we found the nonsynonymous mutations had a frequency distribution of shift to the high frequency (right in the figure), in other words, they had a significant excess (p-value = 0.02, Fisher's test) of higher frequency (> 0.1) mutations compared to the identified synonymous mutations.
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Furthermore, changing the distribution of shifts from one hospital to another will not affect the final exam results.
The distribution of shifts in codon usage for random mutations (SH_r) is shown in Figure 1.
The same offset, gain and shift calculations were performed on each one of 300 bootstrapped tuning curves to produce a distribution of shifts for each neuron from which the 95% CI was calculated by the percentile method.
A Fisher-test for the distribution of a contingency table of AT3 vs. GC3 codons in the left and right panel of this graph reveals a p-value of 5*10-4 5*10-4atindicatingificantly non-random disignificantly shifts.
A non-parametric test was used because although the normalized shifts were normally distributed (Lilliefors test, p > 0.05), the underlying distribution of raw shift values was not normally distributed (Lilliefors test, p = 0.001).
(C ) Scatterplot and marginal distributions of shifts measured using the fronto-parallel plane stimulus during real and simulated pursuit (n = 34 cells).
10.7554/eLife.04693.010 Figure 4. Scatterplot and marginal distributions of shifts measured during real pursuit (RP) and simulated pursuit (SP) using 3D cloud stimuli (n = 72 cells).
A known or assumed distribution of the shift values.
A known or assumed distribution of the shift values. .
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CEO of Professional Science Editing for Scientists @ prosciediting.com