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A panel of ten dinucleotide polymorphic microsatellite markers was selected for genotyping.
A set of 411 polymorphic markers totaling 451 nuclear SNPs (375 SNPs and 36 microhaplotype markers) was selected for the custom probe capture panel.
First, the most informative pair of markers was selected, followed by sequential addition of other markers.
From the 60K SNP, a subset of 6210 markers was selected for this study.
A single clone containing both markers was selected and completely sequenced.
The analysis option of conditioning markers was selected for testing direct association of a single marker in the significant haplotypes.
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For panel selection, markers were selected incrementally.
Cofactor markers were selected by a modified stepwise selection procedure (Buckler et al. 2009).
With more markers available for selection, the possibility of highly collinear markers being selected in the prediction models is greater.
The markers were selected to minimize the number of missing calls as per the selection criterion.
The SNP markers were selected from genome-wide SNP marker data (Ebana et al. 2010).
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