Exploiting CpG hypermutability to identify phenotypically significant variation within human protein-coding genes.

Genome Biol Evol · 2011 · PMC3184784 · PMID 21398426

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likely to be significantno p-value reported

With more columns to be counted, larger genes are more likely to be significant in LRTs.

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nominally significantno p-value reported

The distribution of parameter MLEs from nominally significant alignments were consistent with the elevation of both CpG transition and transversion substitutions.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.