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For each vertex in G′, find the maximal cliques that contain the vertex using the Bron-Kerbosch algorithm [ 20] implemented in igraph package [ 21] and select the largest clique of maximal cliques found for all vertices.
Starting with B1, iterate the selection of the kth cluster B k in Steps 2 to 4. Step 2. For each vertex in G ′, find the maximal cliques that contain the vertex using the Bron-Kerbosch algorithm [ 20 ] implemented in igraph package [ 21 ] and select the largest clique of maximal cliques found for all vertices.
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We next translated the 7,712 assembled cDNA sequences into six possible open reading frames (ORFs), and selected the largest ORF for each sequence.
We calculated the sample size on the basis of literature research in the related domain and analyzing the objective and indexes in this trial by using formula: N = Z α / 2 + Z β σ / δ 2 α = 0.05 Z α / 2 = 1.645, 1 − β = 0.90 Z β = 1.282 We calculated the needed sample size for the main indexes and selected the largest one.
We configured Xlight FTP server and selected the large file more than 1 GB to make a certain downloading process that should continue until handoff completion.
Also, we can improve the accuracy of the solution by selecting the appropriate shape parameters and selecting the large values of N. Results show the high accuracy of method by taking this view that storing in time and memory is another useful property in the Sinc method.
We rejected the hypothetical flux distributions growing at 0.05 hr−1 because it heavily favors product yield over productivity, and selected the large range of 0.1-0.35 hr−1 for strain design.
We rank them using volume and select the three largest ones as the top 3 pockets returned by CASTp.
If negatively correlated SNPs still exist after the recoding algorithm has been applied to this clique, discard the chosen clique and select the next largest one.
Our results indicate the following sequencing study design guidelines which take advantage of the recent advances in genotype imputation methodology: Select the largest and most diverse reference panel for sequencing and genotype as many "anchor" markers as possible.
Based on results from this study, we recommend a few guidelines in designing sequencing studies to take advantage of the recent advances in genotype imputation methodology: Select the largest and most diverse reference panel for sequencing, with respect to both haplotypes and phenotype.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com