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All of the obtained results demonstrate that the proposed method precisely identifies damages by using only the first several modes' data, even when incomplete noisy modal data are considered as input data.
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These methods precisely identified 12 candidate intervals, which are shared by all 5 affected individuals.
Under scenarios of large sample size (greater than 300 taxa) and low tip bias, the BiSSE method accurately and precisely identifies the rate parameters contributing to the observed taxonomic excess.
The above systematic relationship between the eruption style and the correlation pattern enables us to develop a method for precisely identifying eruption styles with high time resolution.
When applied to set of unbound structures of DNA-binding proteins, the proposed method can precisely identify the locations of DNA-binding sites.
What is missing from this highly successful system is a method to precisely identify which genomic variables are the statistically significant drivers of the PCs in genomic data, which in turn identifies the genomic variables associated with the unobserved latent variables.
This method cannot precisely identify the time of diagnosis (as the initial diagnosis might not have been associated with a hospital admission in this period), but when there were multiple hospital episodes for a patient, we chose the earliest date of any hospital admission with the relevant diagnosis code.
However, both methods could precisely identify two time points when topology of the network changes, excluding the case of i = 3.
Given a genetic or metabolic change to algal lipid production, technological advancements will require the development of methods to precisely identify and quantify the lipids generated by microalgae and to correlate the generated lipids to the various genetic manipulation strategies and/or growth conditions [ 6, 7].
The method involves (i) growth selections on a mixture of several different plasmid-based genomic libraries of defined insert sizes or SCALEs, (ii) microarray studies of enriched plasmid DNA, and a (iii) mathematical multiscale analysis that precisely identifies the relevant genetic elements.
We developed a proprietary image-processing algorithm that precisely identifies the irregular cell contour of PC12 cells (Figure 2A), and implemented it as a plug-in for commercial image processing software (see Methods).
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