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An algebra of reconfigurations was defined based on the following primitive reconfiguration operations: const π, par π, join N, split n and remove c, where indexes represent parameters: π is a coordination pattern, N is a set of nodes, n is a node and c is a channel identifier.
Similar(59)
The number of patterns, N, is therefore 1,024 (= 4).
The dissimilarity of a CRMB against a pattern, P n is defined as: (7).
However, TGFβ signalling does not induce N expression in the main body follicular cells, indicating that the spatial pattern of N is independent of TGFβ.
If the continuously matched nucleotides are longer than the shifting length N, at least one repeat with the basic pattern length N is proved to exist in the target sequence.
The pattern [AG]NNATGG (where N is any nucleotide, and letters in square brackets indicate alternative bases at a given position) was used, derived from published data on initiator codons from highly curated sequences [ 15].
Of the covariates, only clay content proved important in explaining spatial differences in response to N. The sinusoidal response pattern of N was similar over the 2 years but the amplitudes varied due to differences in weather.
The exact distributions of the number of runs and patterns are often very hard to obtain or computationally problematic, especially when the pattern is complex and n is very large.
The resulting PDF is given by Here L is the gray level of fully developed speckle pattern without noise and N is the maximum gray level.
The occurrence of 32 possible pentapeptide binary patterns (polar (P /non-polar (N)) is comP /non-polar1 Non-homologous proteis strucomputed
In Figure 8, A and B, Algorithm 1 strongly alters the patterns of diversity as N is decreased.
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