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Unlike longer mutants in our previous study (γ-ΔC21 or longer) (26), we could not find rotation when 0.49- μm beads were attached instead of the 0.29- μm beads.
The failure to find rotation in γ-ΔC40 with 0.29- μm beads, despite the rotation, though very rare, of 40-nm beads attached to γ-ΔN22C43 γ-ΔN22C43o points to a load effect.
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In both groups at 12 months follow-up we found rotations (posterior tilt) around the x-axis as the main rotation pattern.
The Cartesian distance of the orthogonal projection of each MT on the reference plane after rotation was summed, to find the rotation that produced the minimum value.
However, subsequent workers, using the same plates, failed to find any rotation.
In particular, property can be used to find the rotation angle of the image.
Instead of visualization, we find the rotation, translation, and reflection that gives the closest positions to the true locations in the least-squares sense.
We find the rotation angles using an analogy to the technique of composite pulses, which is widely used for control in nuclear magnetic resonance.
By translating the phase-searching problem of the PTS into a real-valued parameter optimization, this study proposes using the RVGA to find a rotation phase vector to reduce PAPR.
The polarization analysis of Phi29 DNA packaging motor did not find a rotation phenomenon either.
To compare the similarity between genetic variation on a PCA plot and geographic maps of sample locations, we used Procrustes analysis to find a rotation that maximizes the similarity (Wang et al. 2012).
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