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 Vol 5: Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts.


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This article is from Frontiers in Genetics, volume 5.AbstractThe goal of this paper is to review recent research on copy number variations (CNVs) and their association with complex and rare diseases. In the latter part of this paper, we focus on how large biorepositories such as the electronic medical record and genomics (eMERGE) consortium may be

Autor: Connolly, John J.; Glessner, Joseph T.; Almoguera, Berta; Crosslin, David R.; Jarvik, Gail P.; Sleiman, Patrick M.; Hakonarson, Hakon

Fuente: https://archive.org/







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