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AnalysisDescription
This dataset is integrated from two of the five original eMERGE site primary datasets into a merged eMERGE dataset. The two original GWAS study phenotypes were Type II Diabetes Mellitus and Cardiac Conduction . DNA samples (N=2634) were genotyped, along with HapMap controls from Coriell, using the Illumina 1M BeadChip at the Broad Institute of MIT and Harvard (\"Broad\").
This dataset is integrated from two of the five original eMERGE site primary datasets into a merged eMERGE dataset. The two original GWAS study phenotypes were Type II Diabetes Mellitus and Cardiac Conduction . DNA samples (N=2634) were genotyped, along with HapMap controls from Coriell, using the Illumina 1M BeadChip at the Broad Institute of MIT and Harvard (\"Broad\").
This project is an integration of the five original eMERGE site primary datasets with additional genotyping for resistant hypertension cases and controls into a merged eMERGE dataset. For this study, we have combined 18,663 individuals from eMERGE. All of these individuals were genotyped using the Illumina 660W-Quadv1_A BeadChip at either the Broad Institute of MIT and Harvard or Center for Inherited Disease (CIDR) at Johns Hopkins. Later specific genome-wide analysis was performed for Red Blood Cells, White Blood Cells, Height, Lipids, Diabetic Retinopathy, Hypothyroidism, Resistant Hypertension, and PheWAS.
This project is an integration of the five original eMERGE site primary datasets with additional genotyping for resistant hypertension cases and controls into a merged eMERGE dataset. For this study, we have combined 18,663 individuals from eMERGE. All of these individuals were genotyped using the Illumina 660W-Quadv1_A BeadChip at either the Broad Institute of MIT and Harvard or Center for Inherited Disease (CIDR) at Johns Hopkins. Later specific genome-wide analysis was performed for Red Blood Cells, White Blood Cells, Height, Lipids, Diabetic Retinopathy, Hypothyroidism, Resistant Hypertension, and PheWAS.

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