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Both populations were evaluated for leaf hairiness at the tillering stage.
Hybrid collections derived from segregating F3 4 lines from both populations were evaluated together with hybrids obtained from their parental lines (repeated 9 times) as well as 2 common checks in field traits using an incomplete 24 × 10 alpha design with two replications.
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The proliferation rate of both populations was evaluated using a cell DNA assay.
In cycles 6, 7 and 8, 50 individuals from both high and low populations were evaluated in order to make selections.
The effects of risk factors on cord blood levels of both infected and non-infected populations were evaluated initially using a two-sample t-test followed by a multiple linear regression model.
Populations were evaluated by colorimetric cell viability assays and morphology by fluorescence imaging.
Sex ratio biases within sampled populations were evaluated using nonparametric Wilcoxon tests.
Following puromycin selection, the transduced populations were evaluated for Timeless knockdown by immunoblotting.
A total of 22 white clover populations were evaluated in the study (Table 1).
Directions of evolution between populations were evaluated as the difference of the averaged FCs per locality.
Thus, a total of 6 phage populations were evaluated for the two antigens phOx- and NIP-BSA.
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