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Five sets of markers were used in this study.
Only non-distorted and less distorted markers were used for mapping studies.
Three molecular markers were used: ITS, atpB-rbcL and trnL-F.
To this end, selected bacterial PLFA markers were used (Additional file 1: Table S1).
The embedded wooden fiducial markers were used for alignment and augmentation of image co-registration.
Fifteen co-dominant markers were used for genotyping of the MBF6-26/2*B MBF6-26/2*B
The 32 landmarks and the 4 fiducial markers were used for superimposition [25],[25].
In total, 147 markers were used for QTL analysis of the RILs.
Seven markers were used to genotype the BC5F3 and BC5F4 populations.
In our study, the predictability plateaued when 5000 markers were used for prediction of all traits.
The markers were used to detect polymorphisms between NIP and '93-11 '93-11
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