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

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...

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Main Authors: Bamshad, Michael J., Shendure, Jay A., Rieder, Mark J., Valle, David, Hamosh, Ada, Lupski, James R., Gibbs, Richard A., Boerwinkle, Eric, Lifton, Rick P., Gerstein, Mark, Gunel, Murat, Mane, Shrikant, Nickersonon, Deborah A.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 2012
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Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3702263/
https://ncbi.nlm.nih.gov/pubmed/22628075
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.35470
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