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These rare cell populations would not have been identified by utilizing a positive selection methodology initially targeting EpCAM.
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These results suggest a positive selection for the earliness allele.
for a positive selection.
We prepared a positive selection marker and a negative selection marker, as shown in Figure 1.
This divergence between nearby markers and even markers in moderate linkage allows for models incorporating H|H to converge when models utilizing other positive selection measures do not.
After a positive selection-driven allele replacement is over, positive selection transforms into negative selection (fig. 1 a ).
We first created a binary vector, named pABr1 (Figure 1a), with the sgfp gene under control of the ToxA promoter from the ascomycete P. tritici-repentis (Ciuffetti et al. [1997]), inserted within the T-DNA region, which also contains the hygromycin phosphotransferase (hph) gene utilized for positive selection of transformants.
These cells were passed through a positive-selection column.
A Long-Rang Haplotype test was utilized to detect recent positive selection.
For the identification of E-selectin specific thioaptamer, we utilized a two-step selection strategy.
This study utilized a selection of fresh fruiting bodies, infected plant tissues, and axenically-cultured fungi (Fig. 2).
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