Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

Researchers have successfully applied exome sequencing to discover causal variants in selected individuals with familial, highly penetrant disorders. We demonstrate the utility of exome sequencing followed by imputation for discovering low-frequency variants associated with complex quantitative trai...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Auer, Paul L., Johnsen, Jill M., Johnson, Andrew D., Logsdon, Benjamin A., Lange, Leslie A., Nalls, Michael A., Zhang, Guosheng, Franceschini, Nora, Fox, Keolu, Lange, Ethan M., Rich, Stephen S., O’Donnell, Christopher J., Jackson, Rebecca D., Wallace, Robert B., Chen, Zhao, Graubert, Timothy A., Wilson, James G., Tang, Hua, Lettre, Guillaume, Reiner, Alex P., Ganesh, Santhi K., Li, Yun
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Elsevier 2012
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3487117/
https://ncbi.nlm.nih.gov/pubmed/23103231
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2012.08.031
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