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We also found that most significant correlations between cis-eQTLs located on different chromosomes can be explained by long-range allelic association.
The absence of an urban rural pattern in total OC pesticide concentrations may be explained by long-range transport of "legacy" pesticides long banned in North America [e.g., DDT (dichlorodiphenyltrichloroethane)] as well as agricultural activities and atmospheric transport of current-use pesticides such as endosulfan and lindane (Gingrich et al. 2001; Harner et al. 2004).
There was no good evidence to distinguish between underlying two-locus and one-locus models (Fig. 5), although the association signal showed two peaks at ∼48.85 Mb (close to rs706793) and at ∼49.45 Mb (very close to rs11169552) that could not readily be explained by long-range LD between these two regions (Supplementary Material, Fig. S1).
Additionally, conservation of gene order in certain regions of the genome has been explained by long-range gene regulation [ 39].
But our results cannot easily be explained by long branch attraction (LBA) effects (contra [ 13]).
In the case of spotted owls, previous observations of California spotted owl haplotypes in the range of northern spotted owls, and vice versa, could be explained by long-distance dispersal or hybridization.
Printzen et al., reported large-scale intraspecific disjunctions in many species that can alternatively be explained by range fragmentation and widespread long-distance dispersal [ 38].
The low correlation may be explained by a range of factors.
This high variation could be explained by a range of natural deformities.
This may be explained by a wide range of exposure within this category (range 50 2100).
Probably this can be explained by the poorer range of motion.
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