ID
45681
Description
Principal Investigator: Nathan O. Stitziel, MD, PhD, McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, USA MeSH: Coronary Artery Disease https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001227 The genetic basis of coronary artery disease in individuals of non-European ancestry is largely unknown. The Washington University Coronary Artery Disease Study (WUCADS) recruited participants of non-European ancestry with and without coronary artery disease to address this question. Whole genome sequencing in WUCADS was performed at the McDonnell Genome Institute at Washington University.
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Versions (1)
- 4/26/23 4/26/23 - Simon Heim
Copyright Holder
Nathan O. Stitziel, MD, PhD, McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, USA
Uploaded on
April 26, 2023
DOI
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Creative Commons BY 4.0
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dbGaP phs001227 Washington University Coronary Artery Disease Study
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and affection status for coronary artery disease.
- This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This subject phenotype table contains subject IDs, gender, race, and age.
- This sample attributes table contains sample IDs, body site where sample was collected, analyte type, histological type, and tumor status.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and affection status for coronary artery disease.
- This data table contains a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This subject phenotype table contains subject IDs, gender, race, and age.
- This sample attributes table contains sample IDs, body site where sample was collected, analyte type, histological type, and tumor status.
C0680251 (UMLS CUI [1,2])
C2985691 (UMLS CUI [1,2])
C0085973 (UMLS CUI [2,1])
C5447420 (UMLS CUI [2,2])
C1518422 (UMLS CUI [2,3])
C0239307 (UMLS CUI [2,4])
C0262926 (UMLS CUI [2,5])
C1956346 (UMLS CUI [2,6])
C0027051 (UMLS CUI [2,7])
C0877341 (UMLS CUI [2,8])
C0242231 (UMLS CUI [2,9])
C0085973 (UMLS CUI [3,1])
C0750501 (UMLS CUI [3,2])
C1658408 (UMLS CUI [3,3])
C0206132 (UMLS CUI [3,4])
C4553389 (UMLS CUI [4,1])
C1518422 (UMLS CUI [4,2])
C0239307 (UMLS CUI [4,3])
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