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Moreover, transferred microsatellites are expected to show a substantial level of null alleles (Oddou-Muratorio et al. 2009).
In addition, such measures calculated using single-copy microsatellites, and those including duplicated palindromic microsatellites, are expected to be very different, thanks to the effects of gene conversion.
Computationally, we used an assumption that, as a reflection of dynamic mutational activity, microsatellites are expected to exhibit significantly higher prevalence of intraspecific polymorphism than nonmicrosatellite repeat loci in the genome.
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Considering the low linkage disequilibrium between marker pairs and their wide genomic distribution [ 37, 40] even the limited number of nuclear markers (seven isozymes and six microsatellites) is expected to reflect genome wide differentiation patterns among the four investigated species.
These microsatellite markers are expected to be useful for studies of the population genetics of P. ishidoyana.
These unigene derived microsatellite (UGMS) markers are expected to possess high inter specific transferability as they belong to relatively conserved regions of the genome.
The focus of this study is mature dinucleotide microsatellites in the human genome, which are expected to be at increased risk for mutation.
Tumors with a high mutation rate, such as melanoma, lung carcinoma, or microsatellite instability (MSI)+ colorectal carcinoma are expected to bear more mutated antigens and are therefore more immunogenic.
The species is octoploid and thus complex fragment patterns are expected using codominant microsatellite markers.
Under the assumption that microsatellites are neutral, no differences between chromosome arrangements or among the same arrangement from different sites are expected by selection on the microsatellite loci themselves.
Then, we searched for long-mer microsatellite accumulation in S. latifolia and S. vulgaris (see Methods), which are expected to be rare in the PAR [ 62].
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