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| 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. |
| 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\"). |