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As both the practice and the terminology become more common, variations emerge.
Amongst the more common variations of R 2 is the adjusted R 2, R 2 adj, which adjusts for the number of variables in the regression equation.
In contrast with these very rare, gene-specific mutations, more common variations in genes (polymorphisms) might cause more subtle variations in DNA repair capacity at the population level, in particular when multiple genes from one pathway are studied [ 109].
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The more common variation is Goldberg, which dropped that central "en" into oblivion.
Thus, it appears that the 5' end polymorphism confined to a few miRNAs is a result of Drosha processing shift while the more common 3'end variations observed in most miRNAs is due to modifications introduced after the Drosha/Dicer processing.
It is possible that the chromosome 17 linkage observed in multiplex PCGP families is because of mutations in a nearby gene, and the more common BRIP1 variations observed by us and others may have more subtle influences on disease susceptibility.
Partial or complete albinism is known in some species, but a more common colour variation is ambicoloration (coloration on both sides).
The potential role of the coding and non-coding BRIP1 SNPs identified in this report remains unclear, as it is possible that a more common genetic variation contributes to PCa risk.
More explicitly, common variation within several genes is thought to confer enhanced susceptibility towards the aforementioned environmental challenges [1].
Variability on the level of gene expression is far more common than nucleotide variations which alter protein sequences and it is believed that these haplotype variations determine individual traits and predispositions for common diseases such as PD.
Efficient approaches to narrow down the possibilities are to sequence more genomes for common variations and system biological investigation using "omic" data [ 45].
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com