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The markers were previously segmented using a threshold-based algorithm.
These vegetal markers were previously considered to have been deposited in the lacustrine system, in restricted isolation.
This allowed the development of a set of PCR-based markers for specific HMW glutenin genes encoding By-subunits for which no markers were previously available.
Primers for each of the 5 markers were previously described [12], [13].
Fifteen SNP markers were previously identified in An. funestus [ 18].
Sequences of the primers for the amplification of those markers were previously reported [ 18].
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Research of RNA viability markers was previously studied for many bacterial species.
A genetic linkage map of M. zebra consisting of 834 RAD-tag markers was previously constructed [ 34].
A preliminary linkage map with AFLP, RFLP and a small number of SSR markers was previously constructed for the tenera parent.
The low polymorphism observed between 'Ferjalou Jalousia®' and 'Fantasia' using AFLP markers was previously reported using RFLP and SSR markers [ 13] and was likely the consequence of the very low genetic distance between these two parental varieties [ 13].
A bony and anatomical landmark based marker-set consisting of 27 retroreflective markers was previously tested to record the patient-specific gait pattern by means of six digital video cameras with a video sample rate of 70 Hz [ 28].
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