Connection Between Epigenome, Selective Mutability, Evolution, and Human Disease
Li, Harris et al., PLoS Genetics
Researchers at the Baylor College of Medicine and elsewhere propose a "connection between the epigenome, selective mutability, evolution, and human disease" based on the findings of their study on associations of structural mutability with germline DNA methylation and with non-allelic homologous recombination mediated by low-copy repeats. "Combined evidence from four human sperm methylome maps, human genome evolution, structural polymorphisms in the human population, and previous genomic and disease studies consistently points to a strong association of germline hypomethylation and genomic instability," the Baylor-led team writes.
Q&A: Vanderbilt Team Harnesses EMRs and Genotyping to Replicate Genotype-Phenotype Associations
"Our aim was to study SNPs previously and reproducibly associated in [genome-wide association studies] with susceptibility to common diseases and to determine whether those associations could be replicated with the use of only the information derived from the EMR to determine case and control status
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