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Microsatellites were able to retrieve the well-established classification into Indica (isozyme group 1), Japonica (group 6, comprising temperate and tropical forms) and specific groups from the Himalayan foothills including some Aus varieties (group 2) and some aromatic varieties (group 5).
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Out of these 300 microsatellites, we were able to detect polymorphism and Mendelian segregation at 237, i.e. 79%, in this particular mapping population.
Despite the widespread feminization of male roach in effluent-contaminated rivers of southern England, using nuclear DNA microsatellites we were able to identify some populations that have been confined to stretches of river with moderate to high exposure to estrogenic effluents over multiple generations.
In most cases, mungbean microsatellite primers were able to amplify DNA of other Vigna species.
Analyzing repeating sequences of DNA called microsatellites, the scientists were able to figure out that the 70 pigeon breeds they studied fell into two groups.
Through microsatellite analysis, we were able to demonstrate that they possessed murine chromosomal DNA (Figure 4F).
Based on the nine microsatellite loci we were able to unambiguously assign paternity of each tadpole to one of the two putative sires.
Through a whole genome scan with microsatellite markers, we were able to map six genomic regions associated with bovine tick resistance.
By examining more closely spaced markers on 1p36 in our microsatellite analysis, we were able to detect interstitial deletion in 12% of our tumour series.
For 24 charadriiform microsatellite loci we were able to design consensus primers with a maximum of three base mismatches per primer pair (sequences are provided in Additional file 1).
Using population surveys and microsatellite markers, they were able to demonstrate at least seven independent transitions from outcrossing to selfing, all of which occurred at the edge of the species range where diversity was lower.
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