We used the strand-oriented reads from the CB IL and YK IL libraries to infer the orientation of the isotigs and singletons.
For the megathrust model, we established the length of the potential source fault from the trench azimuth from 14°N to 18°N, while focal mechanism solutions were used to infer the orientation of the upper-plate fault.
As observers could see how a region shown on the top extended in three dimensions by also looking at the cross-section on the side, we could determine if participants could correctly infer the orientation of extension when given sufficient information to solve the problem.
These results confirm the capability of our model to infer centrosome orientation from microtubule length, which capability was employed above to explain the novel effect of taxol.
Our findings contribute to this growing body of research by highlighting the how gendered expectations of certain groups may facilitate or impair perceivers' ability to infer sexual orientation from gendered cues.
Next, we analyzed whether correlations were observed between helices, in order to infer their orientation with respect to each other.
In this section, we describe the preliminary and final assemblies of the reference transcriptome, and analyses we used to infer the orientation of the resulting isotigs and singletons.
The PFIDO (Phase-Free Inversion Detection Operator) R package (Salm et al. 2012) was then used to infer the orientation of the 8p23 region.
Since it was discovered that the diffusion direction of water molecules could be used to infer the orientation and course of white matter fibre tracts in the brain in vivo, a plethora of studies have been conducted using the diffusion tractography technique.
For the focal mechanism, the kinematic p, b and t axes (Table 3) are used to infer the orientations of the horizontal principal stress axes σ1, σ2 and σ3, respectively (Zoback, 1992).
