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The D3S3045 microsatellite marker was selected because it was found to be informative for the MCM1 donor cells and the MCM3 recipient animal.
One random marker was selected from each bin.
When feasible, a single marker was selected per reference sequence or gene sequence.
In this study, TP53, an important tumor suppressor gene and susceptibility marker, was selected for investigation.
A single, most informative marker was selected from clusters of markers with the purpose to improve QTL mapping.
One SNP marker was selected for further testing based upon its specificity for the Doubs strains (Table 1).
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Cells that had lost the ura4 + marker were selected on yeast extract-based medium containing 5-fluoroorotic acid (5-FOA).
Models of DNA sequence evolution for each marker were selected with the program jModeltest v0.1 [ 132], using the AIC criterion.
A panel of ten dinucleotide polymorphic microsatellite markers was selected for genotyping.
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.
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