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.
HudsonAlpha to use Sequencing to Uncover Genes Responsible for Adverse Drug Response in Parkinson's
"If we could identify a gene, or small set of genes, which determine whether you are at risk for side effects of levodopa, it would really change our [treatment] approach," David Standaert, a neurologist at the University of Alabama, told Clinical Sequencing News.
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