The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.

@article{Bamshad2012TheCF,
  title={The Centers for Mendelian Genomics: a new large-scale initiative to identify the genes underlying rare Mendelian conditions.},
  author={Michael J Bamshad and Jay Shendure and David Valle and Ada Hamosh and James R Lupski and Richard A. Gibbs and Eric Boerwinkle and Richard P. Lifton and Mark Gerstein and Murat Gunel and Shrikant Mane and Deborah A. Nickerson},
  journal={American journal of medical genetics. Part A},
  year={2012},
  volume={158A 7},
  pages={
          1523-5
        }
}
Next generation exome sequencing (ES) and whole genome sequencing (WGS) are new powerful tools for discovering the gene(s) that underlie Mendelian disorders. To accelerate these discoveries, the National Institutes of Health has established three Centers for Mendelian Genomics (CMGs): the Center for Mendelian Genomics at the University of Washington; the Center for Mendelian Genomics at Yale University; and the Baylor-Johns Hopkins Center for Mendelian Genomics at Baylor College of Medicine and… CONTINUE READING
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