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Most of the microsatellite markers used in the present study were originally designed for other genetic linkage maps, allowing us to directly compare each linkage group (LG) among different cichlid groups.
While InSAR does not have good time resolution due to satellite revisit time interval, it can provide high-resolution (1 ~ 10 m) displacement maps, allowing us to make a model of the crustal deformation that accompanied the eruption.
We approached this problem by generating high-resolution deep hairpin bisulfite sequencing (DHBS) maps, allowing us to follow the patterns of symmetric DNA methylation at CpGs dyads on both DNA strands over single replications.
Numerous rounds of manual rebuilding in Coot (Emsley et al., 2010) and refinement in phenix.refine (Adams et al., 2010) against a high resolution native dataset resulted in improved maps, allowing us to manually build the NTDs.
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The metacognitive similarities between concept maps and mind maps allowed us to use the CMA structural scoring system as the foundation for the MMAR.
These maps allow us to draw inferences about the structural organization of the cerebral cortex.
The ROTI maps allow us to estimate the overall fluctuation activity and the auroral oval evolution.
Applying of our method to the global ionosphere maps allows us to obtain additional information about the ionosphere plasma redistribution.
Conformal maps allow us to describe cortical magnification by a scalar field, simply referred to as cortical magnification factor.
These maps allow us to analyze the dependence of the resulting network activity on the properties of network components.
The geographic distribution maps allowed us to identify areas in the various zones that have higher incidence of specific injuries in our county.
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