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Since low errors across the viewing fields were found by averaging left and right errors, it was concluded that this average and should be used in future studies involving relatively small eye-in-head rotations.
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The analogous comparison for the right-hand errors is shown in Figure 3.B (correct notes subtracted from right-hand errors).
Motor execution processes are, however, expected to elicit lateralized EEG potentials [22], [23], which is not consistent with our data: The separate analysis of left-hand and right-hand errors did not reveal any lateralization effect.
To dissociate between a motor and a cognitive explanation, we tested the lateralization of the ERP difference between correct and incorrect keypresses: The ERPs were analyzed separately for left-hand and right-hand errors, with the assumption that motor-related processes of left-hand errors would be reflected in potentials over right-hemispheric motor areas, and vice versa.
In either case, two parallel adaptive filters are implemented to perform the minimization of the left and right error signals independently.
However, this algorithm requires hardware with high specifications, high on complexity, and the effectiveness of this algorithm depends a lot on choosing the right error computation and an appropriate rule base (Reisi et al. 2013).
Error bars are ensemble errors, in all cases, bar the one for the brightest sample (S90 > 1.5 Jy), where three possible error bars: Poissonian (central error bar), analytical estimations for ensemble (left error bar) and bootstrap (right error bar) are shown.
Now, a small clinical trial suggests that even cancer patients with types of tumors that were thought to be impervious to the new drugs could benefit if those malignancies have the right error-riddled DNA signature, a result that could help 3% to 4% of cancer patients.
where (widehat {mathbf {Phi }}_{e} =left [ widehat {Phi }_{e_{l}}~ widehat {Phi }_{e_{r}} right ]^{T}) and (mathbf {Phi }_{n} = left [ Phi _{n_{l}n_{l}} ~ Phi _{n_{r}n_{r}} right ]^{T}) are a concatenation of the left and right error and noise PSDs, respectively.
(F ) Relative chitinase activity mainly detecting endochitinase Cts1 (Koepke et al., 2011 ) in the yeast (left) or hyphal form (right; error bars, s.e.m.; n = 3 independent experiments).
(G ) Bar diagrams depicting amount of Rab5a-Gfp signals per 10 μm hyphae in wt and upa1Δ cells (left, error bars, s.d.; >22 hyphae), as well as amount of Rrm4-Gfp signals per 10 μm hyphae in wt and upa1Δ cells (right, error bars, s.d.; >15 hyphae).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com