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The statistics of changes made by this alignment are provided in Table 2.
The MD displacements suggested by this alignment are azimuthal in character and would suggest a clockwise azimuthal rotation of the MD (looking Z-ward) to reach the strong binding orientation on actin.
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The bpp indicated by this alignment is used by RefAligner to adjust molecule map bpp to 500.
This alignment is scored by interaction similarity and sequence similarity as follows: (i) Aligned node pairs (i, j = π(i)) and (i', j' = π(i')) contribute a positive link score if a link is present both between the pair (i, i') in one network and (j, j') in the other (matching links, such as D' - C' and D* - E* in the example of Figure 1).
This alignment was analysed by maximum likelihood (ML) in MEGA5 [ 67] by applying a Jones-Taylor-Thorton (JTT) model of sequence evolution and taking among-site variation into account using a four-category discrete approximation of a Γ distribution with a portion of invariable sites.
This alignment is complicated by distortions of the tissue which naturally occur during histological treatment, and is particularly difficult to achieve over large cortical areas, such as primate visual areas.
In a real scenario, a spoofing signal has difficulty aligning with an authentic signal carrier received by the target receiver, or achieving this alignment is extremely expensive, e.g., high precision distance measurement technology (radar) can be employed to measure the relative position of the two signals.
This alignment was edited by eye and using the Clustal-W [32] based sub-alignment tool in Mega4 [33].
This alignment is regulated by Vegfc/Vegfr3 signaling.
This alignment is used by default as the sequence alignment.
This alignment was confirmed by scanning electron microscopy (figure 9c, d).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com