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The derivative free optimization results are compared with a gradient based sequential quadratic programming algorithm, but we clearly identify some issues limiting the performance of gradient based algorithms.
In the present work, we clearly identify features of planar microcavity emission that are often overlooked in the literature, namely, an increase in line width with NA (by a factor of 3 in the present samples) and the peak shift of the central emission wavelength as a function of NA and detuning.
So we clearly identify that in the report.
Contrary to sequence-based predictions that implicated the small subunit of the enzyme in determining whether a particular RubisCO species can be sequestered, we clearly identify the large subunit as the key to RubisCO incorporation into carboxysomes.
We clearly identify care services as the senders of the messages, as would have been done in a letter.
However, we clearly identify mutants that in cell culture show aggregation propensities that do not fit with expectations for disease duration.
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In this report, we clearly identified a novel perennial form very close to O. meridionalis and distinct from O. rufipogon.
However, we clearly identified single cells showing two or more TOs with their corresponding electron-dense cores (Fig. 5, arrows).
We clearly identified seven highly conserved blocks alternating with seven variable blocks, as also shown by others [24].
Despite these calculated set-backs, we clearly identified some genetic interactions with SMN in these tests and these will be discussed below.
By using this technology, we clearly identified more than 40,000 informative sequences on V3-V4 16S rRNA gene region from each stool sample, in the present study and this led to the construction of the phylogenetic core of microbiota [16].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com