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The grain size distribution and the number of particles located at grain boundaries were determined as a function of time.
Gene boundaries were determined as follows.
Fragment boundaries were determined as previously described [ 16] and basecalls were made at heterozygous sites previously determined by whole genome sequencing.
The CDS boundaries were determined as follows: the upstream CDS boundary was selected by choosing the most upstream start codon position from the set of isoforms; the downstream CDS boundary was selected by choosing the most upstream stop codon position from the set of isoforms that map to the gene (if more than one authentic stop codon exists, the most upstream stop codon position is chosen.
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Results show that the multi-population genetic algorithm program can be applied in any real-world wind farms for wind turbine layout optimization when the wind farm boundary is determined as well as the local wind condition is obtained.
Stability boundaries are determined as a function of the amplitude and frequency of the support point motion, the rotational speed, damping ratios and eigenfrequencies in the blade and edgewise directions.
The horizontal position of the camera center from the lane boundary is determined as parameter between −50 and 50 for each frame I k.
CMAr boundaries were determined with sulcal landmarks as well as information obtained by intracortical microstimulations performed after each neuronal recording.
In all cases gene boundaries (start and stop codons as well as intron/exon boundaries) were determined through comparison with other plastome annotations rather than via experimental evidence.
Aligned ORF boundaries were determined using the GenBank files as guides and confirmed by visual inspection of the alignments.
Cell boundaries were determined by Voronoi segmentation, using nuclei as seeds and propagating the boundaries using a Riemann metric based on the image gradient (Fig. 1d; Jones et al., 2005).
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