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Each of these sample pools was used to probe a separate microarray chip, and thus the mean expression values for each of the three genotypic groups analyzed is the average of 70 individual larvae.
Since there is no published information on the organic nutrient availability at each of these sample locations, it is difficult to determine if this is also a factor in the coral distribution observed in this study.
More details about each of these sample sites can be found elsewhere [ 27– 29].
While samples were collected for each of these sample media, the number of samples varies by media type.
We can therefore determine the error in the estimated fluorescence per cell by finding the standard deviation of the distribution generated by correcting the fluorescence of the tagged strain by each of these sample r a functions.
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The number of variants which were genotyped as 'heterozygous' with genotype confidence >1 was counted for each of these samples.
For each of these samples a fragment-based DNA methylomes is also presented in.txt format (contains chromosome, start, end, length of the fragment, number of CpG sites in the fragment, count of methylated and methylated CPGs and percentage methylation of the fragment).
On each of these samples, HOG features are calculated and fed to the classifier.
For each of these samples, an array of films with different thicknesses by repeating the coatings and varying the NW concentrations in suspension has been prepared.
For each of these samples, we solve the model starting from the time T to any desired time for predicting the votes, e.g., 24 hours after promotion.
As a consequence, pathway-level consistent enrichment of genes annotated in a gene set within each of these sample-level differentiated gene lists would be biologically relevant to the phenotype being contrasted in the classes under study.
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