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Besides, the genetic composition of the α-gliadin loci needs to be compared across a large series of hexaploid bread wheat cultivars.
Whether this SNP can alter the expression of the UGT1A8 gene or links to other functional loci needs to be verified.
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Firstly, sufficient loci need to be incorporated to obtain enough discriminatory power.
Multi-locus empirical datasets have many more sources of variation that would elevate the number of loci needed to estimate θ accurately.
In addition, the choice of marker type, and the number of loci needed, is a function of the evolutionary history of the populations being investigated [4], [9].
To compare genomes, orthologous loci need to be mapped in the species of interest.
This may involve chromatin remodeling of the loci needed for the respective differentiation (see below).
Thus, population-specific loci need further replication with larger sample sizes.
These loci need further evaluation to clarify their relevance in mOGCT.
These loci need to be expressed throughout germ cell development in order to maintain a functional pool of piRNAs.
This is more suited to clinical genetics where typically only a few critical loci need to be assessed.
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