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Cases 1 and 2 are given as samples in Table 1.
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Based on the new algorithm, a fast and reliable MAPLE procedure is designed and S1,S2,…,S50 are given as sample output of this procedure together with the cpu time.
For learning from label proportions, the training samples are divided into groups and label proportions of samples in each group are given as sample truth, instead of giving the label of each sample in the training set [11].
Geographical position (centroid of the individual coordinates) and altitudinal range of sampled individuals are given as well as DNA ploidy levels with the number of individuals per ploidy level (n) and the total number (N) of individuals investigated per sample site.
To be more precise, the integration is performed by using the function values which are given as discrete sampling data on only part of the boundary.
The trajectory of the target in Fig. 6 is formed by 32 measurements from some type of single radar and its performance parameters are given as follows: the sampling interval T = 2 s, maximum detection range r max = 21 km, range error σ r = 20 m, and azimuth error σ β = 0.5°.
Data are given as number of positive samples with percentages in parentheses.
After performing discrete Fourier transform (DFT) on the received samples, frequency domain-received samples are given as Y_{m}[!k]=C_{m} epsilon,k)*(H_{m}[!k] X_{m}[!k])+Z_{m}[!k], (4).
Values are given as mean ± SEM; sample size (n) is described either in the figure legend or in the Results section.
Analyses of pSTATα pBcr-Abl and pJAK2 levels are given as folds of the sample values versus the α -tubulin values used as a loading control.
Results for kidney cell samples are given as percentage of this standard.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com