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None of the tetra-, penta- or hexa-nucleotide repeat-based markers was polymorphic.
Of the 24 charadriiform microsatellite markers we tested, a median of 7 markers was polymorphic per species (12 charadriiform species tested).
> The majority (2765 of 3880; 71.3%) of the successfully amplified SSR markers was polymorphic across the six representative B. napus cultivars/inbred lines (Table 4).
Preliminary tests on a small panel of C. vestalis wasps from different populations look promising: the large majority of the set of 98 markers amplified, and 10-45% of the markers was polymorphic in individuals collected from the field in the Netherlands or from laboratory crosses (J. G. de Boer; unpublished data).
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Forty of the 52 efficient SSR markers were polymorphic and the polymorphism rate reached 76.92% (40/52) (Table 1).
Among these, 202 markers were polymorphic, amounting to 86.6 % polymorphism.
All of the EPIC markers were polymorphic and showed levels of polymorphism similar to that of the widely used internal transcribed spacer (ITS).
RAD markers are polymorphic loci (i.e., sequences with at least one single-nucleotide polymorphism [SNP]) within or between individuals.
In eight P. umbellatus accessions, eight markers were polymorphic.
Twenty-nine markers were polymorphic and therefore informative for genetic studies while 6 were monomorphic.
Among them, 158 SSR markers were polymorphic between the two parents and were used to construct the genetic linkage map of the RIL population.
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