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In this regard, variation between clusters would be ignorable as compared to variation between individual students.
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The mean of pairwise distances between two clusters would be a compromise between the maximum and the minimum distances, but it turned out to behave much like the minimum distance and was therefore not used.
In the gene cluster model, the expanses of noncoding DNA between gene clusters would be explained mainly on the basis of the degradation of redundant genes, rather than the generation of noncoding DNA through de nouveau insertions.
It is reasonable to suppose that clusters #2 and #4 represent the most contrast groups of samples in the data and the line that stretches between centroids of these clusters would be analogous to the trend we observe in the Mootha et al. data set.
Sequencing of these clusters would be necessary to distinguish between expression and sequence divergence.
Finally, the sizes of clusters would be unequal.
To test to which extent cis-eQTL clusters would be conserved across tissues, we questioned whether regions containing cis-eQTL clusters for cardiac genes would overlap with regions containing cis-eQTL clusters for genes expressed in another tissues (with clusters of cis-eQTLs being defined on the basis of maximum intervals of 250 Mb between each cis-eQTL).
When the clusters have been formed, the nodes in cluster would be arrayed in a list and cluster head would be rotated automatically by the order of list.
The aggregation of the cluster would be reduced.
Instead, if the condition of interest would produce less variability between clusters, ρ would be closer to zero.
The average physical distance between cluster sites would be 200/λ·κ = 150 kb; Fig 4 would now give the CDF for the physical spacing between these sites.
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