In addition, the association between SATB2 expression and immunohistochemical microsatellite instability (MSI) screening status was explored.
The extent of chimerism was explored within two populations of a common coral, Acropora millepora, on the Great Barrier Reef, Australia, by using up to 12 polymorphic DNA microsatellite loci.
Allelic richness per locus per population, partition of the genetic diversity and variation, gene-flow, F-statistics, number of migrants, analysis of molecular variance and factorial correspondence analysis of the microsatellite data, were explored as implemented in GENALEX v6 [66].
However, the mode of microsatellite evolution is yet not fully understood, and the role of interrupting motifs for the stability of microsatellites remains to be explored in more detail.
To the best of our knowledge, in humans, because of the limitations of PCR-based genotyping, the relationship of sequence properties of human microsatellites and properties of microsatellite genetic diversity has yet to be explored in detail.
We hypothesize that much of these significant missing genetic components may be explained by variation in parts of the genome, which have not been explored previously, namely, microsatellite or repetitive DNA loci, notably referred to as "Junk DNA" or more recently "Dark Matter" [ 10].
The primer designing for PCR amplification of desired motifs will facilitate studies on mutability, microsatellite abundance, etc. Association of microsatellites with a particular disease or phenotype may also be explored.
EST and mRNA sequences were explored for the existence of microsatellite repeat motifs since they are potential resources for SSR marker discovery [ 17, 18].
Unlinked autosomal microsatellites in six Jewish and two non-Jewish populations were genotyped, and the relationships among these populations were explored.
Improbabilities to be explored.
