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When boils are clustered, natural saltwater upconing is a function of the total discharge of a boil cluster, whereas the boil-to-boil salinity variations within a cluster are determined by the discharge of individual boils and their position relative to neighboring boils.
Then, all clusters that are at most ε further away than the closest cluster are determined.
After clustering, the center of a cluster and the farthest sample from the center of the cluster are determined.
The diffusion properties of the cluster are determined by the particles composing the cluster's entities.
By using matching score of a cluster, the dominant disease and high frequency plant associated to the cluster are determined.
The perimeter, distance from the origin, angle (degrees), shape and x/y-coordinates of the centroid of the cluster are determined using the same methods employed for regions.
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Another cluster is determined highly likely to be "barks".
The kal/bat biosynthesis gene cluster was determined to a 62 kb genomic region of Pseudomonas fluorescens BCCM_ID9359.
Whether the nucleus is stable or decays to a smaller cluster is determined by its size.
The size of a cluster is determined by the distance between each codeword and the cluster's centroid.
To achieve a practical clustering algorithm, many studies [21 23] have proposed schemes where each cluster is determined sequentially, i.e., a cluster is determined from cells that have not been selected yet.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com