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Study Description

The National Human Genome Research Institute (NHGRI) has funded the Centers for Common Disease Genomics (CCDG), a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to common disease phenotypes and to better understand the general principles of genomic architecture underlying common, complex inherited diseases.

This study contains variant calls derived from the whole genome sequence data of an early-onset coronary artery disease case-control cohort collected by the Cleveland Clinic. Case status was assigned based on the presence of myocardial infarction, coronary artery stenosis greater than 70% in at least one coronary artery, and/or revascularization (coronary angioplasty with or without stent placement or coronary artery bypass grafting) at an early age. For these samples, "early age" is defined as men 60 years of age or younger and women 70 years of age or younger.

  • Study Design:
    • Case-Control
  • Study Type:
    • Case-Control
Authorized Access
Publicly Available Data (Public ftp)

Connect to the public download site. The site contains release notes and manifests. The site also contains data dictionaries, variable summaries, documents, and truncated analyses, whenever available.

Molecular Data
TypeSourcePlatformNumber of Oligos/SNPsSNP Batch IdComment
Sequence Library Construction KAPA Biosystems KAPA Hyper PCR-free N/A N/A
Whole Genome Sequencing Illumina HiSeq X N/A N/A
Selected publications
Diseases/Traits Related to Study (MeSH terms)
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