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The differences in lipid profile that are observed between strains can reflect either genetic characteristic or the lipid profile of the food of the parental population.
They are established with the implicit assumption that desired genes, previously selected through phenotypic evaluation, will be effectively transmitted from the parental population to the offspring.
Therefore, the relative frequencies of the A and B alleles in the gamete pool will be the same as in the parental population, namely p and q respectively.
This differs from allopatric speciation in that the isolated populations are numerically much smaller than the parental population.
Selection against interbreeding with the metal-sensitive parental population produced a gradual change in the flowering time of the metal-resistant plants, which eventually produced complete reproductive isolation.
The 359 RILs served as one parental population.
Individuals belonging to each parental population, i.e. HapMap Yoruba (YRI) and CEPH (CEU), were also typed for these markers.
Thus the examination of parental population groups by CoAIMs is critical to accurately assess continental ancestral proportions.
In the analyses performed here, individuals from the NIGMS and NHGRI Repositories were used as parental population reference groups.
They were established simultaneously from the same parental population, using equivalent MOI transduction with lentiviral vectors that differed only in the 19 nt of the shRNA [37].
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Broad-sense heritability for grain yield was 0.57 for bi-parental population 1 and 0.28 for bi-parental population 2 when all drought and optimum environments were combined.
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