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First, we sought to understand the biological significance of long dinucleotide microsatellites by analyzing their locations within the human genome and identifying the genes harboring such microsatellites within exonic sequences.
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We studied microsatellite instability by analyzing five microsatellite sequences (Gonzalez-Garcia et al. 2000).
They also examined the genetic diversity of bee populations by analyzing microsatellites (short, repetitive DNA sequences that are useful markers of genetic variation in populations).
By analyzing microsatellites, Thulin et al. [ 53] detected a small number of specimens with genotypes consistent with those of F1 hybrids in Sweden.
However, we detected two distinct genetic groups within Europe by analyzing microsatellite data of 298 individuals from 27 populations.
To enhance knowledge about genetic characteristics useful for the conservation and sustainable utilization of genetic resource of this species, microsatellite loci were developed by analyzing a reference transcriptome de novo assembled from RNA-seq data of T. grandis.
By analyzing microsatellite markers adjacent to functional genes, we identified two loci (SOD1 and AGLA17) that are "selection candidate" targets associated with the horned/polled trait in cattle.
However, this study also found a minor contribution of a separate Northern European lineage in several Danish populations, a finding that would be difficult to confirm by analyzing microsatellite DNA markers.
More recently, Vigouroux et al. [5] extended this analysis by analyzing similar microsatellites from 771 additional maize and 5 ssp.
Small-scale genetic differentiation should be determined by analyzing nuclear microsatellites.
In this study, we investigated the origins of triple-mutant Pfdhps alleles by analyzing the microsatellite diversity flanking Pfdhps.
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