The selection of a damage-sensitive and noise-insensitive pattern feature is important for all structural damage identification methods.
The nature of human visual system (HVS), which models the low-pass property of human viewers, is considered in DBS, that human viewers are insensitive to patterns with high spatial frequency.
We further show that this encoding is insensitive to pattern speed, and needs little re-sensitization.
Low-linking constructions such as tough/middle constructions, low adverbial verb constructions, subject and object control constructions, and resultative constructions are insensitive to extraction patterns.
In the island scale, some of LPIs regularly changed with the changes in island area, distance to the mainland, population and GDP, yet ERIs were generally insensitive to landscape pattern.
We suggest that broad occupancy-based intercommunity patterns are insensitive to human land use extent in boreal vascular plants, perhaps because of ubiquity of generalists, low species richness, and history of natural disturbance.
However, the interpretation that group-averaged hemodynamic signals are insensitive to the differential patterns of neural activity elicited by the CS+ vs. CS− (for discussion, see Bach et al., 2011) is not consistent with the present data.
Current approaches for analyzing brain images are based on smooth non-linear transformations to a reference atlas (Davis and Eddy, 2009; Hawrylycz et al., 2011) and may be insensitive to fine local patterns like those emerging from the layered structure of the cerebellum or the spatial distribution of cortical interneurons.
We showed that per gene ML estimation of d N/d S is robust to such sporadic deviations from neutrality and the proteins as a whole remain in the nearly neutral regime, consistent with the fact that whole-gene estimates are insensitive to local selection patterns and are too coarse-grained to detect selection.
