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Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Study
phs001516
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Alpha1-Antitrypsin Deficiency Registry (AADR-BioLINCC)
Study
phs004187
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Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study
Study
phs001844
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ACTIV-6: COVID-19 Outpatient Randomized Trial to Evaluate Efficacy of Repurposed Medications
Study
phs003941
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Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
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Drug Signatures for Prediction and Mitigation of Toxicity
Study
phs002088
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Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study
Study
EGAS00001007363
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This study generated Oxford Nanopore long read sequencing data of cancer cell line mixtures for validating long-read variant calls in cancer genomics
Study
EGAS00001008107
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The data access committee for Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Dac
EGAC00001003253
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Screening for human epigenetic variation at CpG islands
Dataset
EGAD00001000059