the missing story behind genome wide association studies: single nucleotide polymorphisms in gene deserts have a story to tell

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ID: 242677
2014
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Abstract
Genome wide association studies are central to the evolution of personalized medicine. However, the propensity for SNPs to fall outside of genes means that understanding how these polymorphisms alter cellular function requires an expanded view of human genetics. Integrating the study of genome structure (chromosome conformation capture) into its function opens up new avenues of exploration. Changes in the epigenome associated with SNPs in gene deserts will allow us to define complex diseases in a much clearer manner, and usher in a new era of disease pathway exploration.
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schierding2014frontiersthe Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;William Stewart Schierding;Wayne S. Cutfield;Wayne S. Cutfield;Justin Martin O'Sullivan;Justin Martin O'Sullivan
Journal chemical record (new york, ny)
Year 2014
DOI
10.3389/fgene.2014.00039
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