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The marker density required is determined by how quickly linkage disequilibrium (LD) decays in the population.
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The persistency of that accuracy will depend on how quickly those linkage blocks decay over generations.
Despite these limitations, the ability to resolve glycans based on their SA α2-3/α2-6 α2-3/α2-6 α2-3/α2-6 potentialinkagesckly isoffersquantheate these linkage isomers.
HH can also be applied to test known causative genes or loci quickly for potential linkage.
Each mutant SNP is next to its non-mutant control, so that the whole genome can be quickly scanned for linkage.
This has already proven advantageous to our research group, with the composite map being used to quickly identify the linkage relationships of microsatellite markers used in population genetic studies.
Especially, spurious LD [ 9], which is not due to linkage, changes quickly over generations.
This spurious linkage disequilibrium should quickly dissipate with periodic recombination and population growth [32], provided the introduced population has not lost sexual competence.
It has developed quickly to incorporate the routine linkage of a number of strategic, core datasets.
Although QTL mapping should in principle be feasible in wild intraspecific populations (as an alternative to artificial crosses), this approach is less likely to be successful in trees because LD (linkage disequilibrium) will decay quickly in large outbreeding plant populations.
The proportion of identical linkage phases across breeding populations quickly declined with increasing physical distance between markers to values close to 0.5.
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